Allele Registry

Canonical Allele Identifier: PA093377

Gene: H6PD HGNC NCBI

ClinVar RCV:

RCV000017511

RCV001636602

ClinVar Variation:

16131

HGVS (amino-acid)	Matching Registered Transcripts
NP_004276.2:p.Arg453Gln	CA126206 NM_004285.4:c.1358G>A