Canonical Allele Identifier: PA2827947478
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2773631
ClinVar RCV Id: RCV003584487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2486Leu
CA16037559
NM_001354895.2:c.7457C>T