V56G (p.Val56Gly) variant of GBA1 (P04062)
V56G (p.Val56Gly) in GBA1 (P04062) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as no classification for the single variant. The record also includes structural context.
V56G (p.Val56Gly) variant details
- p.Val56Gly
- Ensembl rs878853318
- no classification for the single variant
- Missense
- ClinVar: no classification for the single variant
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available