T47R (p.Thr47Arg) variant of HMGCS2 (P54868)
T47R (p.Thr47Arg) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
T47R (p.Thr47Arg) variant details
- p.Thr47Arg
- TOPMed rs1653157007
- gnomAD rs1653157007
- Missense
- Structural context available