NM_004273.5:c.661C>T

HGVS Expressions

  • NG_012635.1:g.48331C>T
  • NM_004273.5:c.661C>T
  • NP_004264.2:p.Arg221Cys
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Genomic Location

chr10:72007692

Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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