Canonical Allele Identifier: PA2828058038
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722591
ClinVar RCV Id: RCV002305701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Asp282Tyr
CA415235126
NM_001360016.2:c.844G>T