Canonical Allele Identifier: PA2827980785
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1427985
ClinVar RCV Id: RCV003653528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2550del
CA2580613641
NM_001354899.2:c.7648_7650del