N18S (p.Asn18Ser) variant of TNNC1 (P63316)
N18S (p.Asn18Ser) in TNNC1 (P63316) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
N18S (p.Asn18Ser) variant details
- p.Asn18Ser
- TOPMed rs1706343846
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- UniProt: Uncertain significance
- Structural context available