A26D (p.Ala26Asp) variant of HMGCS2 (P54868)
A26D (p.Ala26Asp) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
A26D (p.Ala26Asp) variant details
- p.Ala26Asp
- TOPMed rs1653322892
- Missense
- Structural context available