Canonical Allele Identifier: PA2827344645
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429766
ClinVar RCV Id: RCV001950168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Ala232Ser
CA352229915
NM_001330729.2:c.694G>T