R3T (p.Arg3Thr) variant of CHD2 (O14647)
R3T (p.Arg3Thr) in CHD2 (O14647) is a missense change. The record also includes structural context.
R3T (p.Arg3Thr) variant details
- p.Arg3Thr
- TOPMed rs2052524459
- gnomAD rs2052524459
- Missense
- Structural context available