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Mutations on the Protein: P15538 From Positions: 302 To 327

5
3
0
2


Swiss-Prot Disease: VAR_065667
p.THR318ARG
N/A
N/A
Adrenal hyperplasia 4 (AH4)


Swiss-Prot Disease: VAR_001262
p.THR318MET
N/A
N/A
Adrenal hyperplasia 4 (AH4)


Swiss-Prot Disease: VAR_001263
p.THR319MET
N/A
N/A
Adrenal hyperplasia 4 (AH4)


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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