N69D (p.Asn69Asp) variant of LPA (Apolipoprotein(a))
N69D (p.Asn69Asp) in LPA (Apolipoprotein(a)) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
N69D (p.Asn69Asp) variant details
- p.Asn69Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available