Canonical Allele Identifier: PA2580192132
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 1786732
ClinVar RCV Id: RCV002432452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289617.1:p.Ser98Ala
CA406303547
NM_001302688.2:c.292T>G