Allele Registry

Canonical Allele Identifier: PA127266

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000019140

RCV000087199

RCV000417687

RCV000425010

RCV000427454

RCV000427896

RCV000433199

RCV000435333

RCV000437703

RCV000443060

RCV000443883

ClinVar Variation:

17578

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Asp32Gly	CA127265 NM_001904.4:c.95A>G