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Mutations on the Protein: P10916 From Positions: 17 To 25

4
2
0
2


Swiss-Prot Disease: VAR_004603
p.GLU22LYS
N/A
N/A
Cardiomyopathy, familial hypertrophic 10 (CMH10)


Swiss-Prot Disease: VAR_004602
p.PHE18LEU
N/A
N/A
Cardiomyopathy, familial hypertrophic 10 (CMH10)


OMIM Disease: 160781.0002
p.GLU22LYS
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10


OMIM Disease: 160781.0005
p.PHE18LEU
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 10






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