S19T (p.Ser19Thr) variant of FGFR2 (P21802)
S19T (p.Ser19Thr) in FGFR2 (P21802) is a missense change. The record also includes structural context.
S19T (p.Ser19Thr) variant details
- p.Ser19Thr
- Ensembl rs2135484261
- Missense
- Structural context available