P56H (p.Pro56His) variant of SDHB (P21912)
P56H (p.Pro56His) in SDHB (P21912) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P56H (p.Pro56His) variant details
- p.Pro56His
- NCI-TCGA Cosmic COSV1009
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available