Allele Registry

Canonical Allele Identifier: PA121051

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011158

RCV000066276

ClinVar Variation:

10414

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Tyr352His	CA121049 NM_000402.4:c.1054T>C