NM_001302688.2:c.466T>C

HGVS Expressions

  • NG_007084.2:g.7903T>C
  • NM_001302688.2:c.466T>C
  • NP_001289617.1:p.Cys156Arg

Associated Genes

Apolipoprotein E
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Genomic Location

chr19:44908684

Clinvar Clinical Significance

Association

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

429358

Clinvar

441269

Epidemiology in the Arab World

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