Canonical Allele Identifier: PA916019323
Gene: APOE HGNC NCBI
ClinVar RCV:
RCV000417087
ClinVar Variation:
375636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289617.1:p.Arg180Leu
CA16044403
NM_001302688.2:c.539G>T