U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC114827850, MYL2
(A13T)
Single nucleotide variant
(missense variant)
Primary familial hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
MYH7
(S1776G)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GUncertain significance
MYLK2
(K131E)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
GUncertain significance
MYLK2
(T505I)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
GUncertain significance
Format
Sort by
Choose Destination