A16S (p.Ala16Ser) variant of FGFR2 (P21802)
A16S (p.Ala16Ser) in FGFR2 (P21802) is a missense change. The record also includes structural context.
A16S (p.Ala16Ser) variant details
- p.Ala16Ser
- TOPMed rs984992964
- gnomAD rs984992964
- Missense
- Structural context available