S6T (p.Ser6Thr) variant of LHCGR (P22888)
S6T (p.Ser6Thr) in LHCGR (P22888) is a missense change. The record also includes structural context.
S6T (p.Ser6Thr) variant details
- p.Ser6Thr
- TOPMed rs1670179661
- Missense
- Structural context available
S6T (p.Ser6Thr) in LHCGR (P22888) is a missense change. The record also includes structural context.