Canonical Allele Identifier: PA2827969288
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482374
ClinVar RCV Id: RCV000576021 RCV002526859 RCV003537141 RCV004000979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1846Tyr
CA042401
NM_001354898.2:c.5536G>T