Q99H (p.Gln99His) variant of HMGCS2 (P54868)
Q99H (p.Gln99His) in HMGCS2 (P54868) is a missense change. The record also includes population frequency data and structural context.
Q99H (p.Gln99His) variant details
- p.Gln99His
- 1000Genomes rs147746231
- ESP rs147746231
- ExAC rs147746231
- TOPMed rs147746231
- Missense
- Population evidence available
- Structural context available