E19D (p.Glu19Asp) variant of TNNC1 (P63316)
E19D (p.Glu19Asp) 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.
E19D (p.Glu19Asp) variant details
- p.Glu19Asp
- rs2471444734
- ClinGen CA353169691
- ClinVar RCV004265064
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available