Canonical Allele Identifier: PA2827994099
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 646667
ClinVar RCV Id: RCV003535918 RCV004001639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1059Thr
CA035129
NM_001354901.2:c.3176A>C