E38D (p.Glu38Asp) variant of ATP1A1 (P05023)
E38D (p.Glu38Asp) in ATP1A1 (P05023) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E38D (p.Glu38Asp) variant details
- p.Glu38Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available