NM_000769.4:c.636G>A

HGVS Expressions

  • NG_008384.3:g.22973G>A
  • NM_000769.4:c.636G>A
  • NP_000760.1:p.Trp212Ter
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Genomic Location

chr10:94780653

Clinvar Clinical Significance

Drug Response

CTGA Clinical Significance

Drug Response

Variant Type

Substitution

dbSNP

4986893

Clinvar

16899

Epidemiology in the Arab World

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