Allele Registry

Canonical Allele Identifier: PA120991

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011118

ClinVar Variation:

10387

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Arg257Leu	CA120990 NM_000402.4:c.770G>T CA2580573397 NM_000402.4:c.[770G>T;466A>G]