Canonical Allele Identifier: PA2827986780
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1037892
ClinVar RCV Id: RCV003538713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1596Asn
CA16032084
NM_001354900.2:c.4786G>A