Canonical Allele Identifier: PA2828007655
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3014066
ClinVar RCV Id: RCV003875705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ala1571Val
CA16032680
NM_001354905.2:c.4712C>T