G19V (p.Gly19Val) variant of ATP6V1A (P38606)
G19V (p.Gly19Val) in ATP6V1A (P38606) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
G19V (p.Gly19Val) variant details
- p.Gly19Val
- Ensembl rs972975431
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available