A2E (p.Ala2Glu) variant of CHM (P24386)
A2E (p.Ala2Glu) in CHM (P24386) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A2E (p.Ala2Glu) variant details
- p.Ala2Glu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available