R89G (p.Arg89Gly) variant of SLC2A1 (P11166)
R89G (p.Arg89Gly) in SLC2A1 (P11166) is a missense change. The record also includes structural context.
R89G (p.Arg89Gly) variant details
- p.Arg89Gly
- Ensembl rs961569873
- Missense
- Structural context available