C9F (p.Cys9Phe) variant of FGFR2 (P21802)
C9F (p.Cys9Phe) in FGFR2 (P21802) is a missense change. The record also includes structural context.
C9F (p.Cys9Phe) variant details
- p.Cys9Phe
- Ensembl rs2135485570
- Missense
- Structural context available
C9F (p.Cys9Phe) in FGFR2 (P21802) is a missense change. The record also includes structural context.