D39G (p.Asp39Gly) variant of LHCGR (P22888)
D39G (p.Asp39Gly) in LHCGR (P22888) is a missense change. The record also includes structural context.
D39G (p.Asp39Gly) variant details
- p.Asp39Gly
- Ensembl rs2103767146
- Missense
- Structural context available