Allele Registry

Canonical Allele Identifier: PA130189

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000030892

RCV000507037

RCV000991016

RCV003460496

ClinVar Variation:

37203

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Asp211Val	CA033058 NM_000402.4:c.[632A>T;466A>G] CA130188 NM_000402.4:c.632A>T