NM_000053.3:c.2231T>C

HGVS Expressions

  • NG_008806.1:g.58060T>C
  • NM_000053.3:c.2231T>C
  • NP_000044.2:p.Ser744Pro
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Genomic Location

Chr13:51958431

Variant Type

Substitution

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