Y53H (p.Tyr53His) variant of ATP1A2 (P50993)
Y53H (p.Tyr53His) in ATP1A2 (P50993) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y53H (p.Tyr53His) variant details
- p.Tyr53His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available