G6PD A- NM_001360016.2:c.[202G>A;376A>G]

HGVS Expressions

  • NG_009015.2:g.[16571G>A;17296A>G]
  • NM_001360016.2:c.[202G>A;376A>G]
  • NP_001346945.1:p.[Val68Met;Asn126Asp]
  • NC_000023.11:g.154536002C>T(;)154535277T>C
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Clinvar Clinical Significance

Likely Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Haplotype

Clinvar

10361

Epidemiology in the Arab World

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