S26G (p.Ser26Gly) variant of FGFR2 (P21802)
S26G (p.Ser26Gly) in FGFR2 (P21802) is a missense change. The record also includes structural context.
S26G (p.Ser26Gly) variant details
- p.Ser26Gly
- Ensembl rs2135483314
- Missense
- Structural context available