N47K (p.Asn47Lys) variant of HMGCR (P04035)
N47K (p.Asn47Lys) in HMGCR (P04035) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
N47K (p.Asn47Lys) variant details
- p.Asn47Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available