Canonical Allele Identifier: PA2825525365
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1318448
ClinVar RCV Id: RCV001753223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Tyr254Cys
CA352230089
NM_001098210.2:c.761A>G