NM_000243.3:c.2078_2080TGA[1]

HGVS Expressions

  • NG_007871.1:g.18219_18221TGA[1]
  • NM_000243.3:c.2078_2080TGA[1]
  • NP_000234.1:p.Met694del
Back to search Result
Genomic Location

chr16:3243405-3243407

Clinvar Clinical Significance

Pathogenic

Variant Type

Deletion

Clinvar

2556

© CAGS 2024. All rights reserved.