Canonical Allele Identifier: PA916019322
Gene: APOE HGNC NCBI
ClinVar RCV:
RCV000019430
ClinVar Variation:
17850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001289617.1:p.Arg180Ser
CA127501
NM_001302688.2:c.538C>A