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Mutations on the Protein: P19429 From Positions: 137 To 147

7
4
0
3


Swiss-Prot Disease: VAR_019872
p.ARG141GLN
N/A
N/A
Cardiomyopathy, familial hypertrophic 7 (CMH7)


Swiss-Prot Disease: VAR_007603
p.ARG145GLY
N/A
N/A
Cardiomyopathy, familial hypertrophic 7 (CMH7)


Swiss-Prot Disease: VAR_016080
p.ARG145TRP
N/A
N/A
Cardiomyopathy, familial restrictive 1 (RCM1)


Swiss-Prot Disease: VAR_016079
p.LEU144GLN
N/A
N/A
Cardiomyopathy, familial restrictive 1 (RCM1)


OMIM Disease: 191044.0001
p.ARG145GLY
N/A
N/A
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7


OMIM Disease: 191044.0008
p.ARG145TRP
N/A
N/A
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1


OMIM Disease: 191044.0010
p.LEU144GLN
N/A
N/A
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1






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