R46G (p.Arg46Gly) variant of SRD5A2 (P31213)
R46G (p.Arg46Gly) in SRD5A2 (P31213) is a missense change. The record also includes structural context.
R46G (p.Arg46Gly) variant details
- p.Arg46Gly
- TOPMed rs914715976
- Missense
- Structural context available