Allele Registry

Canonical Allele Identifier: PA645495862

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417825

RCV000418863

RCV000425263

RCV000426101

RCV000426401

RCV000433600

RCV000434673

RCV000435028

RCV000436119

RCV000442478

RCV000443305

ClinVar Variation:

376391

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Ser33Pro	CA16602830 NM_001904.4:c.97T>C