Canonical Allele Identifier: PA127272
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Asp32Tyr
CA127271
NM_001904.4:c.94G>T