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Mutations on the Protein: P61764 From Positions: 178 To 208

2
1
0
1


Swiss-Prot Disease: VAR_046206
p.CYS180TYR
N/A
N/A
Epileptic encephalopathy, early infantile, 4 (EIEE4)


OMIM Disease: 602926.0002
p.CYS180TYR
N/A
N/A
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 4






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