NM_001010892.3:c.368del

HGVS Expressions

  • NG_012934.1:g.5513del
  • NM_001010892.3:c.368del
  • NP_001010892.1:p.Pro123LeufsTer44
  • NC_000006.12:g.116616991del
Back to search Result
CTGA Clinical Significance

Pathogenic

Variant Type

Deletion

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.