Canonical Allele Identifier: PA099141
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Ser33Tyr
CA127263
NM_001098209.1:c.98C>A