Canonical Allele Identifier: PA2827344642
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800539
ClinVar RCV Id: RCV002461678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Phe225_Lys226delinsLeuArg
CA2580069821
NM_001330729.2:c.675_677delinsAAG