Canonical Allele Identifier: PA099141
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17577
ClinVar RCV Id: RCV000019138 RCV000019139 RCV000423917 RCV000435233 RCV000426112 RCV000443472 RCV000435972 RCV000418289 RCV000430278 RCV000434171 RCV000424968 RCV000437025 RCV000443834 RCV000444481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Ser33Tyr
CA127263
NM_001098209.1:c.98C>A