Canonical Allele Identifier: PA916040478
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411500
ClinVar RCV Id: RCV000569027 RCV001775818 RCV002523392 RCV002481467 RCV004001964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala1689Thr
CA16032296
NM_001354896.2:c.5065G>A