Canonical Allele Identifier: PA2573223468
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403651
ClinVar RCV Id: RCV001909157

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Gly268Glu
CA352230187
NM_001904.4:c.803G>A