Canonical Allele Identifier: PA2741890513
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2653693
ClinVar RCV Id: RCV003437772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Ser23Gly
CA352228073
NM_001904.4:c.67A>G