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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GYPC, LOC129934706
(S15N)
Single nucleotide variant
(5 prime UTR variant +1 more)
Blood group, Gerbich system
GUncertain significance
GYPC
(P16T +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(P24R +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(E29D +2 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
GYPC
(I35K +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
+2 more
GUncertain significance
GYPC
(V44A +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(I45M +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(V51I +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(R61C +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(Y64F +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(R65L +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
GYPC
(K67Q +2 more)
Single nucleotide variant
(missense variant)
Blood group, Gerbich system
GUncertain significance
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