NM_000577.4:c.336T>C

HGVS Expressions

  • NG_021240.1:g.19835T>C
  • NM_000577.4:c.336T>C
  • NP_000568.1:p.Ser112=
  • NC_000002.12:g.113132727T>C
Back to search Result
Clinvar Clinical Significance

Benign

CTGA Clinical Significance

Benign

Variant Type

Substitution

dbSNP

315952

Clinvar

330827

Epidemiology in the Arab World

View Map
© CAGS 2025. All rights reserved.