Canonical Allele Identifier: PA2827999389
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411478
ClinVar RCV Id: RCV000457741 RCV000571502 RCV000759449 RCV001706640 RCV003743726 RCV004001957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg2655His
CA049981
NM_001354901.2:c.7964G>A