Canonical Allele Identifier: PA2828022613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438880
ClinVar RCV Id: RCV000506358 RCV000558695 RCV002289692 RCV000580492 RCV001591152 RCV003743766 RCV004003533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val1322Met
CA16031876
NM_001354906.2:c.3964G>A