Allele Registry

Canonical Allele Identifier: PA2827344531

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419361

RCV000420492

RCV000420998

RCV000421620

RCV000429634

RCV000430785

RCV000431858

RCV000432982

RCV000438660

RCV000441059

RCV000441660

ClinVar Variation:

375894

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317658.1:p.Ser30Tyr	CA16602377 NM_001330729.2:c.89C>A