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Links from MedGen

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAP2
(R13Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy, dilated, 2I
GUncertain significance
CAP2
(M1T)
Single nucleotide variant
(missense variant +1 more)
Cardiomyopathy, dilated, 2I
GUncertain significance
CAP2
(C318fs +2 more)
Deletion
Cardiomyopathy, dilated, 2I
GPathogenic
CAP2
(Y316* +2 more)
Single nucleotide variant
Cardiomyopathy, dilated, 2I
GPathogenic
CAP2
Single nucleotide variant
Cardiomyopathy, dilated, 2I
GPathogenic
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