R66L (p.Arg66Leu) variant of ATP13A2 (Q9NQ11)
R66L (p.Arg66Leu) in ATP13A2 (Q9NQ11) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R66L (p.Arg66Leu) variant details
- p.Arg66Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available