Allele Registry

This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.

Canonical Allele Identifier: PA121003

Gene: G6PD HGNC NCBI

ClinVar RCV:

RCV000011129

RCV000011130

ClinVar Variation:

10394

HGVS (amino-acid)	Matching Registered Transcripts
NP_000393.4:p.Arg228Pro	CA121002 NM_000402.4:c.683G>C