Mutations on the Protein: NP_001021384 From Positions: 0 To 22
OMIM Disease: 610613.0001 
p.ARG1HIS
N/A
| |
N/A
|
|---|
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY
|
|---|
OMIM Disease: 610613.0015 
p.TYR1TER
N/A
| |
N/A
|
|---|
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE||DEFICIENCY
|
|---|
: 
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
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2
0
0
2
