Allele Registry

Canonical Allele Identifier: PA2827344528

Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000418083

RCV000419419

RCV000420040

RCV000426895

RCV000427501

RCV000427907

RCV000430713

RCV000436663

RCV000438184

RCV000438599

RCV000438776

RCV000444074

RCV003332169

ClinVar Variation:

376232

376233

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317658.1:p.Gly27Arg	CA16602685 NM_001330729.2:c.79G>A CA16602686 NM_001330729.2:c.79G>C