Canonical Allele Identifier: PA2825525362
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522021
ClinVar RCV Id: RCV002028029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Met243Ile
CA352229942
NM_001098210.2:c.729G>A
CA352229943
NM_001098210.2:c.729G>C
CA352229944
NM_001098210.2:c.729G>T