L41P (p.Leu41Pro) variant of TNNC1 (P63316)
L41P (p.Leu41Pro) in TNNC1 (P63316) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
L41P (p.Leu41Pro) variant details
- p.Leu41Pro
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available