A39T (p.Ala39Thr) variant of HMGCS2 (P54868)
A39T (p.Ala39Thr) in HMGCS2 (P54868) is a missense change. The record also includes structural context.
A39T (p.Ala39Thr) variant details
- p.Ala39Thr
- gnomAD rs1208729772
- Missense
- Structural context available