Canonical Allele Identifier: PA2827344659
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403651
ClinVar RCV Id: RCV001909157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Gly261Glu
CA352230187
NM_001330729.2:c.782G>A