R16T (p.Arg16Thr) variant of HMGCS2 (P54868)
R16T (p.Arg16Thr) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
R16T (p.Arg16Thr) variant details
- p.Arg16Thr
- ExAC rs773898985
- TOPMed rs773898985
- gnomAD rs773898985
- Missense
- Structural context available