Canonical Allele Identifier: PA099098
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17581
ClinVar RCV Id: RCV000019144 RCV000128842 RCV000420526 RCV000418154 RCV000419388 RCV000426162 RCV000426839 RCV000430774 RCV000438170 RCV000437074 RCV000441036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091679.1:p.Asp32Tyr
CA127271
NM_001098209.1:c.94G>T