A15G (p.Ala15Gly) variant of VHL (P40337)
A15G (p.Ala15Gly) in VHL (P40337) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A15G (p.Ala15Gly) variant details
- p.Ala15Gly
- gnomAD rs1159027899
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available