E37D (p.Glu37Asp) variant of FGFR2 (P21802)
E37D (p.Glu37Asp) in FGFR2 (P21802) is a missense change. The record also includes structural context.
E37D (p.Glu37Asp) variant details
- p.Glu37Asp
- Ensembl rs2135125167
- cosmic curated COSV10966
- Missense
- Structural context available