Home News About DMDM Database Statistics Research Publications Contact  

Mutations on the Protein: P56178 From Positions: 173 To 188

2
1
0
1




Swiss-Prot Disease: VAR_067413
p.GLN178PRO
N/A
N/A
Split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive (SHFM1D)


OMIM Disease: 600028.0001
p.GLN178PRO
N/A
N/A
SPLIT-HAND/FOOT MALFORMATION 1 WITH SENSORINEURAL HEARING LOSS, AUTOSOMAL||RECESSIVE (1 family)






   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258