Allele Registry

Canonical Allele Identifier: PA645495867

Gene: CTNNB1 HGNC NCBI

ClinVar RCV:

RCV000419447

RCV000427084

RCV000427731

RCV000430157

RCV000436689

RCV000437750

RCV000442160

RCV000442184

ClinVar Variation:

376390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Gly34Ala	CA16602829 NM_001904.4:c.101G>C