Y56H (p.Tyr56His) variant of ABCC1 (P33527)
Y56H (p.Tyr56His) in ABCC1 (P33527) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Y56H (p.Tyr56His) variant details
- p.Tyr56His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available