NM_003620.4:c.275G>C

HGVS Expressions

  • NG_023265.1:g.5497G>C
  • NM_003620.4:c.275G>C
  • NP_003611.1:p.Cys92Ser
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Genomic Location

chr17:60600689

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Epidemiology in the Arab World

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