C56Y (p.Cys56Tyr) variant of FGFR4 (P22455)
C56Y (p.Cys56Tyr) in FGFR4 (P22455) is a missense change. The record also includes structural context.
C56Y (p.Cys56Tyr) variant details
- p.Cys56Tyr
- ESP rs150191035
- ExAC rs150191035
- TOPMed rs150191035
- gnomAD rs150191035
- Missense
- Structural context available