A89D (p.Ala89Asp) variant of PRPH2 (Peripherin-2)
A89D (p.Ala89Asp) in PRPH2 (Peripherin-2) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A89D (p.Ala89Asp) variant details
- p.Ala89Asp
- NCI-TCGA Cosmic COSV5783
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available