Mutations on the Protein: NP_937799 From Positions: 146 To 155
OMIM Disease: 608537.0024 
p.HIS150ASP
N/A
| |
N/A
|
|---|
ERYTHROCYTOSIS, FAMILIAL, 2
|
|---|
OMIM Disease: 608537.0014 
p.LEU147VAL
N/A
| |
N/A
|
|---|
VON HIPPEL-LINDAU SYNDROME||ERYTHROCYTOSIS, FAMILIAL, 2, INCLUDED;;||PHEOCHROMOCYTOMA, INCLUDED
|
|---|
OMIM Disease: 608537.0023 
p.PRO151SER
N/A
| |
N/A
|
|---|
ERYTHROCYTOSIS, FAMILIAL, 2
|
|---|
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 |
|
3
0
0
3
