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Mutations on the Protein: P15538 From Positions: 352 To 377

3
1
0
2


Swiss-Prot Disease: VAR_001264
p.ARG374GLN
N/A
N/A
Adrenal hyperplasia 4 (AH4)


OMIM Disease: 610613.0017
p.ALA368ASP
N/A
N/A
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY


OMIM Disease: 610613.0004
p.ARG374GLN
N/A
N/A
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY






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