Allele Registry

Canonical Allele Identifier: PA120966

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011094

RCV002305427

ClinVar Variation:

10373

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Phe246Leu	CA120965 NM_000402.4:c.738T>G CA415236892 NM_000402.4:c.738T>A CA415236910 NM_000402.4:c.736T>C