cardiomyopathy MYH7 mutation (E848G)
DiseaseAssertion: cardiomyopathy
Variant: NM_000257.4:c.2543A>G
ClinVar: 177758
CAID: CA012584
cardiomyopathy MYH7 mutation (E848G)
DiseaseAssertion: cardiomyopathy
Variant: NM_000257.4:c.2543A>G
ClinVar: 177758
CAID: CA012584