Canonical Allele Identifier: PA2573081197
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318448
ClinVar RCV Id: RCV001753223

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Tyr254Cys
CA352230089
NM_001904.4:c.761A>G