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Mutations on the Protein: Q8WXF7 From Positions: 195 To 223

3
2
0
1



Swiss-Prot Disease: VAR_017146
p.ARG217GLN
N/A
N/A
Spastic paraplegia 3, autosomal dominant (SPG3)


Swiss-Prot Polymorphism: VAR_067656
p.TYR196CYS
N/A
N/A
N/A


OMIM Disease: 606439.0004
p.ARG217GLN
N/A
N/A
SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT






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