S137T (p.Ser137Thr) variant of ATP1A3 (P13637)
S137T (p.Ser137Thr) in ATP1A3 (P13637) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
S137T (p.Ser137Thr) variant details
- p.Ser137Thr
- rs2514079536
- ClinGen CA406055429
- ClinVar RCV003223832
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance (in AHC2)
- UniProt: Uncertain significance (in AHC2)
- Structural context available