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Mutations on the Protein: NP_001243196 From Positions: 0 To 66

1
0
0
1


OMIM Disease: 608517.0004
p.TYR20CYS
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 22||CARDIOMYOPATHY, DILATED, 1KK, INCLUDED


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