L18F (p.Leu18Phe) variant of CHM (P24386)
L18F (p.Leu18Phe) 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.
L18F (p.Leu18Phe) variant details
- p.Leu18Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available