Canonical Allele Identifier: PA916019328
Gene: APOE HGNC NCBI

Linked Data

ClinVar Variation Id: 17857
ClinVar RCV Id: RCV000019440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289617.1:p.Lys190Glu
CA127506
NM_001302688.2:c.568A>G