Canonical Allele Identifier: PA099182
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17587
ClinVar RCV Id: RCV000019152 RCV000422057 RCV000427656 RCV000426659 RCV000432291 RCV000436836 RCV000442251 RCV000442963 RCV000443038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Thr41Ile
CA127281
NM_001098209.1:c.122C>T