D69E (p.Asp69Glu) variant of HMGCS2 (P54868)
D69E (p.Asp69Glu) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
D69E (p.Asp69Glu) variant details
- p.Asp69Glu
- ESP rs142709072
- ExAC rs142709072
- TOPMed rs142709072
- gnomAD rs142709072
- Missense
- Structural context available