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Mutations on the Protein: NP_001159434 From Positions: 0 To 39

2
0
0
2


OMIM Disease: 605367.0006
p.ARG1TER
N/A
N/A
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 17


OMIM Disease: 605367.0001
p.SER1LEU
N/A
N/A
PROSTATE CANCER, HEREDITARY, 2






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