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Mutations on the Protein: Q9H1R3 From Positions: 60 To 89

3
1
1
1


Swiss-Prot Disease: VAR_014197
p.ALA87VAL
N/A
N/A
Cardiomyopathy, familial hypertrophic (CMH)


dbSNP Polymorphism: rs115398036
p.GLY89ASP
N/A
N/A
N/A


OMIM Disease: 606566.0001
p.ALA87VAL
N/A
N/A
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC






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