Canonical Allele Identifier: PA645398789
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411364
ClinVar RCV Id: RCV000483155 RCV000764559 RCV000575683 RCV004001922 RCV003535729 RCV002525602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gln264Arg
CA049479
NM_001127510.3:c.791A>G