NM_006231.4:c.3890C>T

HGVS Expressions

  • NG_033840.1:g.43104C>T
  • NM_006231.4:c.3890C>T
  • NP_006222.2:p.Ser1297Leu

Associated Genes

Polymerase, DNA, Epsilon
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Genomic Location

chr12:132649421

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

240486

Epidemiology in the Arab World

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