Canonical Allele Identifier: PA2580260817
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1942640
ClinVar RCV Id: RCV002675937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Thr297Met
CA2330982
NM_001904.4:c.890C>T