C17S (p.Cys17Ser) variant of HSD17B3 (P37058)
C17S (p.Cys17Ser) in HSD17B3 (P37058) is a missense change. The record also includes structural context.
C17S (p.Cys17Ser) variant details
- p.Cys17Ser
- TOPMed rs868469733
- gnomAD rs868469733
- Missense
- Structural context available