Canonical Allele Identifier: PA127278
Gene: CTNNB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 17584
ClinVar RCV Id: RCV000019149 RCV000423249 RCV000426491 RCV000422250 RCV000433938 RCV000434538 RCV000432939 RCV000439589 RCV000443977 RCV000443851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001895.1:p.Gly34Glu
CA127277
NM_001904.4:c.101G>A