APOE*3 Allele NM_000041.4:c.[388=;526=]

HGVS Expressions

  • NG_007084.2:g.[7903=;8041=]
  • NM_000041.4:c.[388=;526=]
  • NP_000032.1:p.[Cys130=;Arg176=]
  • NC_000019.10:g.[44908684=;44908822=]

Associated Genes

Apolipoprotein E
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CTGA Clinical Significance

Risk factor, Uncertain Significance

Variant Type

Haplotype

Clinvar

17863

Epidemiology in the Arab World

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