Allele Registry

Canonical Allele Identifier: PA645495849

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421306

RCV000423696

RCV000425710

RCV000431551

RCV000432187

RCV000432497

RCV000438971

RCV000441401

RCV000444118

RCV000444402

RCV002221234

ClinVar Variation:

376228

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Asp32Asn	CA16602681 NM_001904.4:c.94G>A