Mutations on the Protein: NP_000070 From Positions: 206 To 229
OMIM Disease: 100690.0008 
p.PHE208VAL
N/A
| |
N/A
|
|---|
MYASTHENIC SYNDROME, CONGENITAL, FAST-CHANNEL
|
|---|
OMIM Disease: 100690.0006 
p.VAL224PHE
N/A
| |
N/A
|
|---|
MYASTHENIC SYNDROME, CONGENITAL, SLOW-CHANNEL
|
|---|
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 |
|
2
0
0
2
