NM_002691.4:c.2257T>C

HGVS Expressions

  • NG_033800.1:g.34426T>C
  • NM_002691.4:c.2257T>C
  • NP_002682.2:p.Tyr753His
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Genomic Location

chr19:50413748

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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