NM_032444.4:c.3337G>C

HGVS Expressions

  • NG_028123.1:g.26284G>C
  • NM_032444.4:c.3337G>C
  • NP_115820.2:p.Gly1113Arg
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Genomic Location

chr16:3590301

Clinvar Clinical Significance

Uncertain Significance

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

1038292

Epidemiology in the Arab World

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