Canonical Allele Identifier: PA2827971913
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486790
ClinVar RCV Id: RCV000571058 RCV003403364 RCV003459407 RCV003235295 RCV004001190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2644Arg
CA16038725
NM_001354898.2:c.7931C>G