V76F (p.Val76Phe) variant of HSD17B3 (P37058)
V76F (p.Val76Phe) in HSD17B3 (P37058) is a missense change. The record also includes structural context.
V76F (p.Val76Phe) variant details
- p.Val76Phe
- TOPMed rs1825569712
- Missense
- Structural context available