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Mutations on the Protein: NP_001121185 From Positions: 249 To 277

2
0
0
2




OMIM Disease: 606439.0003
p.HIS258ARG
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT


OMIM Disease: 606439.0002
p.SER259TYR
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT






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