Allele Registry

Canonical Allele Identifier: PA645495859

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420132

RCV000423241

RCV000424341

RCV000428518

RCV000430905

RCV000433324

RCV000433966

RCV000439171

RCV000440476

RCV000441600

RCV000443586

ClinVar Variation:

376392

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Ser33Ala	CA16602831 NM_001904.4:c.97T>G