A52T (p.Ala52Thr) variant of SDHB (P21912)
A52T (p.Ala52Thr) in SDHB (P21912) is a missense change. The record also includes structural context.
A52T (p.Ala52Thr) variant details
- p.Ala52Thr
- TOPMed rs1183722041
- gnomAD rs1183722041
- Missense
- Structural context available