Allele Registry

Canonical Allele Identifier: PA121007

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011132

RCV000011133

ClinVar Variation:

10396

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Arg417Cys	CA121006 NM_000402.4:c.1249C>T CA2580573390 NM_000402.4:c.[1249C>T;466A>G]