Allele Registry

Canonical Allele Identifier: PA099170

Gene: CTNNB1 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000019151

RCV000420061

RCV000425340

RCV000426489

RCV000427490

RCV000428583

RCV000433883

RCV000436738

RCV000437726

RCV000442576

RCV000444520

RCV000445320

ClinVar Variation:

17586

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001091679.1:p.Ser37Phe	CA127279 NM_001098209.1:c.110C>T