Canonical Allele Identifier: PA2825524893
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429766
ClinVar RCV Id: RCV001950168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Ala239Ser
CA352229915
NM_001098209.1:c.715G>T