Canonical Allele Identifier: PA2825525208
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 444598
ClinVar RCV Id: RCV000513017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Met14Val
CA2330855
NM_001098210.2:c.40A>G