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Mutations on the Protein: P68133 From Positions: 0 To 19

3
2
0
1






Swiss-Prot Disease: VAR_062424
p.ASP3TYR
N/A
N/A
Nemaline myopathy 3 (NEM3)


Swiss-Prot Disease: VAR_011680
p.GLY17ARG
N/A
N/A
Myopathy, actin, congenital, with excess of thin myofilaments (MPCETM)


OMIM Disease: 102610.0003
p.GLY15ARG
N/A
N/A
MYOPATHY, ACTIN, CONGENITAL, WITH EXCESS OF THIN MYOFILAMENTS


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