Canonical Allele Identifier: PA2828054009
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1478972
ClinVar RCV Id: RCV002579516
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His492Pro
CA16025590
NM_001354905.2:c.1475A>C