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Mutations on the Protein: P49773 From Positions: 88 To 95

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2
0
2



Swiss-Prot Disease: VAR_069216
p.GLY93ASP
N/A
N/A
Neuromyotonia and axonal neuropathy, autosomal recessive (NMAN)


Swiss-Prot Disease: VAR_069215
p.GLY89VAL
N/A
N/A
Neuromyotonia and axonal neuropathy, autosomal recessive (NMAN)


OMIM Disease: 601314.0007
p.GLY93ASP
N/A
N/A
NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE


OMIM Disease: 601314.0003
p.GLY89VAL
N/A
N/A
NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE






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