Allele Registry

Canonical Allele Identifier: PA121011

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011136

RCV000011137

ClinVar Variation:

10398

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Gly440Asp	CA121010 NM_000402.4:c.1319G>A