NM_004260.4:c.3184C>T

HGVS Expressions

  • NG_016430.1:g.10631C>T
  • NM_004260.4:c.3184C>T
  • NP_004251.4:p.Arg1062Trp

Associated Genes

RECQ Protein-Like 4
Back to search Result
Genomic Location

chr8:144512196

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

135145

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.