NM_145045.5:c.850C>T

HGVS Expressions

  • NG_041777.1:g.14526C>T
  • NM_145045.5:c.850C>T
  • NP_659482.3:p.Gln284Ter
  • NC_000019.10:g.11426257G>A
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CTGA Clinical Significance

Likely Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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