Allele Registry

Canonical Allele Identifier: PA916013507

Gene: H6PD HGNC NCBI

ClinVar RCV:

RCV000017511

RCV001636602

ClinVar Variation:

16131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269516.1:p.Arg464Gln	CA126206 NM_001282587.2:c.1391G>A