Allele Registry

Canonical Allele Identifier: PA120987

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011115

RCV002305433

RCV003323355

ClinVar Variation:

10385

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Pro383Ser	CA120986 NM_000402.4:c.1147C>T