Canonical Allele Identifier: PA2825524795
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Ser45del
CA250690
NM_001098209.1:c.133_135del
CA645533084
NM_001098209.1:c.134_136del