P39R (p.Pro39Arg) variant of FGFR2 (P21802)
P39R (p.Pro39Arg) in FGFR2 (P21802) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
P39R (p.Pro39Arg) variant details
- p.Pro39Arg
- Ensembl rs2135124832
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available