Loire NM_000558.5:c.265G>T

HGVS Expressions

  • NG_059186.1:g.5448G>T
  • NM_000558.5:c.265G>T
  • NP_000549.1:p.Ala89Ser
Back to search Result
Genomic Location

chr16:177098

Clinvar Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

15776

© CAGS 2024. All rights reserved.