Canonical Allele Identifier: PA2828001390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1799283
ClinVar RCV Id: RCV002444130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp927Ala
CA16028018
NM_001354902.2:c.2780A>C