Canonical Allele Identifier: PA2580110952
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722678
ClinVar RCV Id: RCV002305788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Pro439Ser
CA415233941
NM_000402.4:c.1315C>T