NM_004415.4:c.2723G>A

HGVS Expressions

  • NG_008803.1:g.39750G>A
  • NM_004415.4:c.2723G>A
  • NP_004406.2:p.Arg908His

Associated Genes

Desmoplakin
Back to search Result
Genomic Location

chr6:7576386

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

Clinvar

177781

Epidemiology in the Arab World

View Map
Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
609040.1Lebanon1Likely BenignRefaat et al. 2019
© CAGS 2024. All rights reserved.