L19H (p.Leu19His) variant of RAD51D (O75771)
L19H (p.Leu19His) in RAD51D (O75771) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
L19H (p.Leu19His) variant details
- p.Leu19His
- TOPMed rs1044486334
- gnomAD rs1044486334
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available