Canonical Allele Identifier: PA099159
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17579
ClinVar RCV Id: RCV000019141 RCV000030945 RCV000087195 RCV000430788 RCV000423597 RCV000438791 RCV000422240 RCV000431366 RCV000421574 RCV000432924 RCV000441696 RCV000445258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Ser37Cys
CA127267
NM_001098209.1:c.110C>G