NM_000789.3:c.2328G>A

HGVS Expressions

  • NG_011648.1:g.16598G>A
  • NM_000789.3:c.2328G>A
  • NP_000780.1:p.Thr776=
  • NC_000017.11:g.63488670G>A
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Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Association

Variant Type

Substitution

dbSNP

4343

Clinvar

256803

Epidemiology in the Arab World

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