G6PD A+ NM_001360016.2:c.376A>G

HGVS Expressions

  • NG_009015.2:g.17296A>G
  • NM_001360016.2:c.376A>G
  • NP_001346945.1:p.Asn126Asp
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Genomic Location

chrX:154535277

Clinvar Clinical Significance

Benign, Likely Benign, Likely Pathogenic, Uncertain Significance

Variant Type

Substitution

dbSNP

1050829

Clinvar

100055

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