Canonical Allele Identifier: PA2827998760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759598
ClinVar RCV Id: RCV002394098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2467Gln
CA16037798
NM_001354901.2:c.7401T>A
CA16037799
NM_001354901.2:c.7401T>G