Allele Registry

Canonical Allele Identifier: PA2827344530

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000019146

RCV000149120

RCV000417805

RCV000418024

RCV000418475

RCV000425225

RCV000427137

RCV000428985

RCV000429363

RCV000435058

RCV000436574

RCV000437867

ClinVar Variation:

17582

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001317658.1:p.Gly27Val	CA127273 NM_001330729.2:c.80G>T CA3047154996 NM_001330729.2:c.80_81delinsTT