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Mutations on the Protein: P38935 From Positions: 0 To 50

2
1
0
1



Swiss-Prot Disease: VAR_058497
p.LEU17PRO
N/A
N/A
Neuronopathy, distal hereditary motor, 6 (HMN6)


OMIM Disease: 600502.0004
p.GLN41TER
N/A
N/A
DISTAL SPINAL MUSCULAR ATROPHY, AUTOSOMAL RECESSIVE, 1






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