Allele Registry

Canonical Allele Identifier: PA645495869

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419464

RCV000419658

RCV000424491

RCV000426018

RCV000430355

RCV000430984

RCV000435198

RCV000435831

RCV000436705

RCV000444358

ClinVar Variation:

376235

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Ser37Ala	CA16602688 NM_001904.4:c.109T>G