Canonical Allele Identifier: PA2827994978
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411418
ClinVar RCV Id: RCV000571708 RCV002461206 RCV004001940 RCV003651859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His1316Arg
CA037682
NM_001354901.2:c.3947A>G