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Mutations on the Protein: Q86TC9 From Positions: 0 To 66

2
1
0
1


Swiss-Prot Disease: VAR_069642
p.TYR20CYS
N/A
N/A
Cardiomyopathy, dilated 1KK (CMD1KK)


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


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