R11G (p.Arg11Gly) variant of SLC47A1 (Q96FL8)
R11G (p.Arg11Gly) in SLC47A1 (Q96FL8) is a missense change. The record also includes structural context.
R11G (p.Arg11Gly) variant details
- p.Arg11Gly
- TOPMed rs1042708808
- Missense
- Structural context available