R56H (p.Arg56His) variant of NFKB1 (P19838)
R56H (p.Arg56His) in NFKB1 (P19838) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
R56H (p.Arg56His) variant details
- p.Arg56His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available