Allele Registry

Canonical Allele Identifier: PA2828057980

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011094

RCV002305427

ClinVar Variation:

10373

HGVS (amino-acid)	Matching Registered Transcripts
NP_001346945.1:p.Phe216Leu	CA120965 NM_001360016.2:c.648T>G CA415236892 NM_001360016.2:c.648T>A CA415236910 NM_001360016.2:c.646T>C