A32G (p.Ala32Gly) variant of SDHB (P21912)
A32G (p.Ala32Gly) in SDHB (P21912) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A32G (p.Ala32Gly) variant details
- p.Ala32Gly
- Ensembl rs1570958135
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available