E37G (p.Glu37Gly) variant of FGFR2 (P21802)
E37G (p.Glu37Gly) in FGFR2 (P21802) is a missense change. The record also includes structural context.
E37G (p.Glu37Gly) variant details
- p.Glu37Gly
- Ensembl rs2135125229
- Missense
- Structural context available