Allele Registry

Canonical Allele Identifier: PA127268

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000019141

RCV000030945

RCV000087195

RCV000421574

RCV000422240

RCV000423597

RCV000430788

RCV000431366

RCV000432924

RCV000438791

RCV000441696

RCV000445258

ClinVar Variation:

17579

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001895.1:p.Ser37Cys	CA127267 NM_001904.4:c.110C>G