NM_006297.3:c.839G>A

HGVS Expressions

  • NG_033799.1:g.28319G>A
  • NM_006297.3:c.839G>A
  • NP_006288.2:p.Arg280His
Back to search Result
Genomic Location

chr19:43552260

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

25489

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.