Allele Registry

Canonical Allele Identifier: PA2828058038

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV002305701

ClinVar Variation:

1722591

HGVS (amino-acid)	Matching Registered Transcripts
NP_001346945.1:p.Asp282Tyr	CA415235126 NM_001360016.2:c.844G>T