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Mutations on the Protein: P49821 From Positions: 325 To 348

2
1
0
1




Swiss-Prot Disease: VAR_008846
p.ALA341VAL
N/A
N/A
Mitochondrial complex I deficiency (MT-C1D)


OMIM Disease: 161015.0003
p.ALA341VAL
N/A
N/A
MITOCHONDRIAL COMPLEX I DEFICIENCY






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