Canonical Allele Identifier: PA2827999034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470112
ClinVar RCV Id: RCV000572911 RCV002527879 RCV001558793 RCV003742799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2552Lys
CA049276
NM_001354901.2:c.7655C>A