A34G (p.Ala34Gly) variant of RAD51D (O75771)
A34G (p.Ala34Gly) in RAD51D (O75771) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
A34G (p.Ala34Gly) variant details
- p.Ala34Gly
- TOPMed rs876658968
- gnomAD rs876658968
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available