R47G (p.Arg47Gly) variant of KCNB1 (Q14721)
R47G (p.Arg47Gly) in KCNB1 (Q14721) is a missense change. The record also includes structural context.
R47G (p.Arg47Gly) variant details
- p.Arg47Gly
- 1000Genomes rs551083482
- ExAC rs551083482
- TOPMed rs551083482
- gnomAD rs551083482
- Missense
- Structural context available