N18K (p.Asn18Lys) variant of TNNC1 (P63316)
N18K (p.Asn18Lys) in TNNC1 (P63316) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
N18K (p.Asn18Lys) variant details
- p.Asn18Lys
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available