NM_000112.4:c.1721T>C

  1. Home
  2. NM_000112.4:c.1721T>C

HGVS Expressions

  • NG_007147.2:g.22432T>C
  • NM_000112.4:c.1721T>C
  • NP_000103.2:p.Ile574Thr
  • NC_000005.10:g.149981314T>C

Associated Genes

Solute Carrier Family 26 (Sulfate Transporter), Member 2
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Likely Benign

Variant Type

Substitution

dbSNP

30832

Clinvar

196209

Epidemiology in the Arab World

View Map
Download Table

Contributors

  • Asha Deepthi: 04.02.2025

Edit History

  • Asha Deepthi: 04.02.2025
Back to search Result
© CAGS 2025. All rights reserved.
© CAGS 2025. All rights reserved.