A37S (p.Ala37Ser) variant of HADHB (P55084)
A37S (p.Ala37Ser) in HADHB (P55084) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
A37S (p.Ala37Ser) variant details
- p.Ala37Ser
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available