E66V (p.Glu66Val) variant of MCM2 (P49736)
E66V (p.Glu66Val) in MCM2 (P49736) is a missense change. The record also includes structural context.
E66V (p.Glu66Val) variant details
- p.Glu66Val
- TOPMed rs1343512840
- Missense
- Structural context available
E66V (p.Glu66Val) in MCM2 (P49736) is a missense change. The record also includes structural context.