Canonical Allele Identifier: PA2827344507
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120980
ClinVar RCV Id: RCV003048931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.His17Leu
CA352228449
NM_001330729.2:c.50A>T