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Mutations on the Protein: NP_001021384 From Positions: 306 To 328

2
0
0
2




OMIM Disease: 610613.0003
p.THR318MET
N/A
N/A
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY


OMIM Disease: 610613.0008
p.THR319MET
N/A
N/A
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY






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