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Mutations on the Protein: P02708 From Positions: 217 To 241

2
0
0
2


OMIM Disease: 100690.0001
p.ASN217LYS
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL


OMIM Disease: 100690.0008
p.PHE233VAL
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, FAST-CHANNEL






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