A19G (p.Ala19Gly) variant of RELN (Reelin)
A19G (p.Ala19Gly) in RELN (Reelin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
A19G (p.Ala19Gly) variant details
- p.Ala19Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.