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Mutations on the Protein: P11230 From Positions: 251 To 276

2
0
0
2



OMIM Disease: 100710.0002
p.LEU263MET
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL


OMIM Disease: 100710.0001
p.VAL266MET
N/A
N/A
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL






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