M13T (p.Met13Thr) variant of SDHAF2 (Q9NX18)
M13T (p.Met13Thr) in SDHAF2 (Q9NX18) is a missense change. The record also includes structural context.
M13T (p.Met13Thr) variant details
- p.Met13Thr
- TOPMed rs1862008982
- Missense
- Structural context available