C9G (p.Cys9Gly) variant of FGFR2 (P21802)
C9G (p.Cys9Gly) in FGFR2 (P21802) is a missense change. The record also includes structural context.
C9G (p.Cys9Gly) variant details
- p.Cys9Gly
- TOPMed rs1479661228
- Missense
- Structural context available
C9G (p.Cys9Gly) in FGFR2 (P21802) is a missense change. The record also includes structural context.