S26T (p.Ser26Thr) variant of FGFR2 (P21802)
S26T (p.Ser26Thr) in FGFR2 (P21802) is a missense change. The record also includes structural context.
S26T (p.Ser26Thr) variant details
- p.Ser26Thr
- gnomAD rs1379302733
- Missense
- Structural context available
S26T (p.Ser26Thr) in FGFR2 (P21802) is a missense change. The record also includes structural context.