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Mutations on the Protein: P15538 From Positions: 25 To 50

3
1
1
1


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


Swiss-Prot Disease: VAR_001260
p.PRO42SER
N/A
N/A
Adrenal hyperplasia 4 (AH4)


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






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