V109G (p.Val109Gly) variant of IDH2 (P48735)
V109G (p.Val109Gly) in IDH2 (P48735) is a missense change. The record also includes structural context.
V109G (p.Val109Gly) variant details
- p.Val109Gly
- 1000Genomes rs2151551241
- Missense
- Structural context available