A16P (p.Ala16Pro) variant of FGFR2 (P21802)
A16P (p.Ala16Pro) in FGFR2 (P21802) is a missense change. The record also includes structural context.
A16P (p.Ala16Pro) variant details
- p.Ala16Pro
- TOPMed rs984992964
- gnomAD rs984992964
- Missense
- Structural context available