NM_000455.5:c.1211C>T

HGVS Expressions

  • NG_007460.2:g.42150C>T
  • NM_000455.5:c.1211C>T
  • NP_000446.1:p.Ser404Phe
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Genomic Location

chr19:1226556

Clinvar Clinical Significance

Benign, Likely Benign

CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

Clinvar

127700

Epidemiology in the Arab World

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