Canonical Allele Identifier: PA2825524890
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_001091679.1:p.Phe232_Lys233delinsLeuArg
CA2580069821
NM_001098209.1:c.696_698delinsAAG