A16G (p.Ala16Gly) variant of FGFR2 (P21802)
A16G (p.Ala16Gly) in FGFR2 (P21802) is a missense change. The record also includes structural context.
A16G (p.Ala16Gly) variant details
- p.Ala16Gly
- Ensembl rs2135484727
- Missense
- Structural context available