Canonical Allele Identifier: PA2827344649
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522021
ClinVar RCV Id: RCV002028029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Met236Ile
CA352229942
NM_001330729.2:c.708G>A
CA352229943
NM_001330729.2:c.708G>C
CA352229944
NM_001330729.2:c.708G>T