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Mutations on the Protein: Q8WXF7 From Positions: 251 To 279

5
3
0
2



Swiss-Prot Disease: VAR_017148
p.HIS258ARG
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_017149
p.SER259TYR
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Disease: VAR_067657
p.VAL253ILE
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


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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