P11H (p.Pro11His) variant of PMS2 (P54278)
P11H (p.Pro11His) in PMS2 (P54278) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
P11H (p.Pro11His) variant details
- p.Pro11His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available