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Mutations on the Protein: P19429 From Positions: 168 To 179

4
2
0
2


Swiss-Prot Disease: VAR_016081
p.ALA171THR
N/A
N/A
Cardiomyopathy, familial restrictive 1 (RCM1)


Swiss-Prot Disease: VAR_016082
p.LYS178GLU
N/A
N/A
Cardiomyopathy, familial restrictive 1 (RCM1)


OMIM Disease: 191044.0011
p.ALA171THR
N/A
N/A
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1


OMIM Disease: 191044.0007
p.LYS178GLU
N/A
N/A
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1






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