NM_032043.3:c.3571A>G

HGVS Expressions

  • NG_007409.2:g.185085A>G
  • NM_032043.3:c.3571A>G
  • NP_114432.2:p.Ile1191Val
Back to search Result
Genomic Location

chr17:61683475

Clinvar Clinical Significance

Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

186989

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.