S138V (p.Ser138Val) variant of HMGCS2 (P54868)
S138V (p.Ser138Val) in HMGCS2 (P54868) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S138V (p.Ser138Val) variant details
- p.Ser138Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available