NM_032444.4:c.5501A>G

HGVS Expressions

  • NG_028123.1:g.34239A>G
  • NM_032444.4:c.5501A>G
  • NP_115820.2:p.Asn1834Ser
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Genomic Location

chr16:3582346

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

241697

Epidemiology in the Arab World

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