Canonical Allele Identifier: PA2825525355
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800539
ClinVar RCV Id: RCV002461678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Phe232_Lys233delinsLeuArg
CA2580069821
NM_001098210.2:c.696_698delinsAAG