P147T (p.Pro147Thr) variant of HSD17B3 (P37058)
P147T (p.Pro147Thr) in HSD17B3 (P37058) is a missense change. The record also includes structural context.
P147T (p.Pro147Thr) variant details
- p.Pro147Thr
- TOPMed rs1002934063
- gnomAD rs1002934063
- Missense
- Structural context available