P52S (p.Pro52Ser) variant of TNNC1 (P63316)
P52S (p.Pro52Ser) in TNNC1 (P63316) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
P52S (p.Pro52Ser) variant details
- p.Pro52Ser
- rs2471444623
- ClinGen CA353168555
- ClinVar RCV003341687
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available