Canonical Allele Identifier: PA2826873389
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 1764810
ClinVar RCV Id: RCV002373776 RCV003138235
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289618.1:p.Trp294Cys
CA9506112
NM_001302689.2:c.882G>T
CA406305758
NM_001302689.2:c.882G>C