Canonical Allele Identifier: PA2828058129
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1685831
ClinVar RCV Id: RCV002249998
ClinVar Variation Id: 1722615
ClinVar RCV Id: RCV002305725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Phe381Leu
CA415234130
NM_001360016.2:c.1143C>G
CA415234131
NM_001360016.2:c.1143C>A
CA415234136
NM_001360016.2:c.1141T>C