Canonical Allele Identifier: PA2828047979
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1485763
ClinVar RCV Id: RCV003745494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr2388Asn
CA16037722
NM_001354904.2:c.7163C>A