Canonical Allele Identifier: PA121050
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 10414
ClinVar RCV Id: RCV000011158 RCV000066276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035810.1:p.Tyr322His
CA121049
NM_001042351.2:c.964T>C