Allele Registry

Canonical Allele Identifier: PA2825161198

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV002305762

ClinVar Variation:

1722652

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Arg111Cys	CA10566297 NM_000402.4:c.331C>T