A56S (p.Ala56Ser) variant of CHRNA4 (P43681)
A56S (p.Ala56Ser) in CHRNA4 (P43681) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
A56S (p.Ala56Ser) variant details
- p.Ala56Ser
- NCI-TCGA Cosmic COSV6471
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.