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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CMC2
(E112K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CMC2
(K58R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CMC2
(N55K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
CMC2
(R42W +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CMC2
(H44D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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