Canonical Allele Identifier: PA2825524907
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403651
ClinVar RCV Id: RCV001909157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Gly268Glu
CA352230187
NM_001098209.1:c.803G>A