Canonical Allele Identifier: PA2827943001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2567009
ClinVar RCV Id: RCV003306858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser1128Tyr
CA16028746
NM_001354895.2:c.3383C>A