Canonical Allele Identifier: PA2825525211
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 635460
ClinVar RCV Id: RCV000786916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Glu15Lys
CA352228024
NM_001098210.2:c.43G>A