Canonical Allele Identifier: PA2828058138
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 10396
ClinVar RCV Id: RCV000011132 RCV000011133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001346945.1:p.Arg387Cys
CA121006
NM_001360016.2:c.1159C>T
CA2580573390
NM_001360016.2:c.[1159C>T;376A>G]