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Mutations on the Protein: P02708 From Positions: 265 To 289

3
1
0
2


Swiss-Prot Disease: VAR_021206
p.PHE278VAL
N/A
N/A
Myasthenic syndrome, congenital, fast-channel (FCCMS)


OMIM Disease: 100690.0005
p.SER269ILE
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL


OMIM Disease: 100690.0007
p.VAL285ILE
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, FAST-CHANNEL






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