P38Q (p.Pro38Gln) variant of FGFR2 (P21802)
P38Q (p.Pro38Gln) in FGFR2 (P21802) is a missense change. The record also includes structural context.
P38Q (p.Pro38Gln) variant details
- p.Pro38Gln
- gnomAD rs1248875226
- Missense
- Structural context available
P38Q (p.Pro38Gln) in FGFR2 (P21802) is a missense change. The record also includes structural context.