Allele Registry

Canonical Allele Identifier: PA120997

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011125

RCV000066262

RCV001267397

RCV002305586

ClinVar Variation:

10390

986140

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Asn393Lys	CA120996 NM_000402.4:c.1179C>A CA415234252 NM_000402.4:c.1179C>G