Canonical Allele Identifier: PA2827344527
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376390
ClinVar RCV Id: RCV000419447 RCV000427084 RCV000427731 RCV000430157 RCV000436689 RCV000437750 RCV000442184 RCV000442160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Gly27Ala
CA16602829
NM_001330729.2:c.80G>C