A19T (p.Ala19Thr) variant of HSD17B3 (P37058)
A19T (p.Ala19Thr) in HSD17B3 (P37058) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A19T (p.Ala19Thr) variant details
- p.Ala19Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available