Canonical Allele Identifier: PA2580192182
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 1796422
ClinVar RCV Id: RCV002441796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289620.1:p.Ser94Trp
CA406303716
NM_001302691.2:c.281C>G