Allele Registry

Canonical Allele Identifier: PA121009

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011134

RCV000011135

ClinVar Variation:

10397

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Val424Leu	CA121008 NM_000402.4:c.1270G>C CA415234049 NM_000402.4:c.1270G>T