Canonical Allele Identifier: PA2827993068
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411558
ClinVar RCV Id: RCV000468198 RCV000491212 RCV000677778 RCV001549488 RCV003651896 RCV003899932 RCV004001982 RCV003479129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg746Gln
CA031897
NM_001354901.2:c.2237G>A