D56N (p.Asp56Asn) variant of LRP2 (P98164)
D56N (p.Asp56Asn) in LRP2 (P98164) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D56N (p.Asp56Asn) variant details
- p.Asp56Asn
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available