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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASAP2, LOC126806133
(E397D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASAP2, LOC126806133
(A441V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASAP2, LOC126806133
(I423V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASAP2, LOC126806133
(T431M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASAP2, LOC126806133
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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