Allele Registry

Canonical Allele Identifier: PA645495863

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418116

RCV000420531

RCV000424580

RCV000425706

RCV000427045

RCV000431206

RCV000432938

RCV000435335

RCV000437702

RCV000440157

RCV000441880

ClinVar Variation:

376393

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Ser33Thr	CA16602832 NM_001904.4:c.97T>A