Canonical Allele Identifier: PA2827344669
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3062030
ClinVar RCV Id: RCV003985140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317658.1:p.Lys285Asn
CA352230348
NM_001330729.2:c.855A>C
CA352230349
NM_001330729.2:c.855A>T