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Mutations on the Protein: Q12768 From Positions: 695 To 753

2
1
0
1



Swiss-Prot Disease: VAR_069985
p.GLY696ALA
N/A
N/A
Spastic paraplegia 8, autosomal dominant (SPG8)


OMIM Disease: 610657.0005
p.GLY696ALA
N/A
N/A
SPASTIC PARAPLEGIA 8, AUTOSOMAL DOMINANT






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