Canonical Allele Identifier: PA250691
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Ser45del
CA250690
NM_001904.4:c.133_135del
CA645533084
NM_001904.4:c.134_136del