T17P (p.Thr17Pro) variant of FGFR2 (P21802)
T17P (p.Thr17Pro) in FGFR2 (P21802) is a missense change. The record also includes structural context.
T17P (p.Thr17Pro) variant details
- p.Thr17Pro
- TOPMed rs1417346628
- gnomAD rs1417346628
- Missense
- Structural context available