Canonical Allele Identifier: PA2827344522
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17583
ClinVar RCV Id: RCV000019147 RCV000019148 RCV000418596 RCV000438845 RCV000439964 RCV000428161 RCV000420986 RCV000505658 RCV000443180 RCV000421635 RCV000423964 RCV000434049 RCV000437352 RCV003332083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Ser26Phe
CA127275
NM_001330729.2:c.77C>T