A66D (p.Ala66Asp) variant of APOC2 (Apolipoprotein C-II)
A66D (p.Ala66Asp) in APOC2 (Apolipoprotein C-II) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A66D (p.Ala66Asp) variant details
- p.Ala66Asp
- NCI-TCGA Cosmic COSV5299
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available