S13N (p.Ser13Asn) variant of MCM2 (P49736)
S13N (p.Ser13Asn) in MCM2 (P49736) is a missense change. The record also includes structural context.
S13N (p.Ser13Asn) variant details
- p.Ser13Asn
- TOPMed rs2074287537
- Missense
- Structural context available
S13N (p.Ser13Asn) in MCM2 (P49736) is a missense change. The record also includes structural context.