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Mutations on the Protein: P02708 From Positions: 145 To 169

2
0
0
2


OMIM Disease: 100690.0004
p.GLY153SER
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL


OMIM Disease: 100690.0002
p.VAL156MET
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL






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