V13F (p.Val13Phe) variant of FGFR2 (P21802)
V13F (p.Val13Phe) in FGFR2 (P21802) is a missense change. The record also includes structural context.
V13F (p.Val13Phe) variant details
- p.Val13Phe
- Ensembl rs2135485083
- Missense
- Structural context available