Allele Registry

Canonical Allele Identifier: PA2580110801

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV002305701

ClinVar Variation:

1722591

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Asp312Tyr	CA415235126 NM_000402.4:c.934G>T