Canonical Allele Identifier: PA2827996056
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469990
ClinVar RCV Id: RCV000679062 RCV002341386 RCV003742726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1646Ala
CA16032508
NM_001354901.2:c.4936A>G