Canonical Allele Identifier: PA2827959602
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_001341826.1:p.Thr1715Ala
CA16032508
NM_001354897.2:c.5143A>G