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Mutations on the Protein: O75880 From Positions: 166 To 181

2
1
0
1





Swiss-Prot Disease: VAR_012109
p.PRO174LEU
N/A
N/A
Mitochondrial complex IV deficiency (MT-C4D)


OMIM Disease: 603644.0002
p.PRO174LEU
N/A
N/A
HEPATIC FAILURE, EARLY-ONSET, AND NEUROLOGIC DISORDER DUE TO CYTOCHROME||c OXIDASE DEFICIENCY






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