Allele Registry

Canonical Allele Identifier: PA2828057987

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011118

ClinVar Variation:

10387

HGVS (amino-acid)	Matching Registered Transcripts
NP_001346945.1:p.Arg227Leu	CA120990 NM_001360016.2:c.680G>T CA2580573397 NM_001360016.2:c.[680G>T;376A>G]