Canonical Allele Identifier: PA2828058039
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 10372
ClinVar RCV Id: RCV000011092 RCV000011093 RCV000180200 RCV000757322 RCV000763204 RCV001166655 RCV003466847 RCV003904827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Asp282His
CA120963
NM_001360016.2:c.844G>C