P12H (p.Pro12His) variant of CDKN1A (P38936)
P12H (p.Pro12His) in CDKN1A (P38936) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
P12H (p.Pro12His) variant details
- p.Pro12His
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.