Canonical Allele Identifier: PA2580110790
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722587
ClinVar RCV Id: RCV002305697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Pro306Ser
CA415235198
NM_000402.4:c.916C>T