Canonical Allele Identifier: PA2825525242
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17582
ClinVar RCV Id: RCV000019146 RCV000149120 RCV000417805 RCV000418024 RCV000418475 RCV000425225 RCV000428985 RCV000427137 RCV000429363 RCV000435058 RCV000436574 RCV000437867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001091680.1:p.Gly34Val
CA127273
NM_001098210.2:c.101G>T