V37F (p.Val37Phe) variant of CHM (P24386)
V37F (p.Val37Phe) 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.
V37F (p.Val37Phe) variant details
- p.Val37Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available