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Mutations on the Protein: NP_001021384 From Positions: 22 To 44

2
0
1
1




dbSNP Polymorphism: rs4534
p.ARG43GLN
N/A
N/A
N/A


OMIM Disease: 610613.0009
p.PRO42SER
N/A
N/A
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY






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