Canonical Allele Identifier: PA2580111132
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722688
ClinVar RCV Id: RCV002305798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Gly518Val
CA415232140
NM_000402.4:c.1553G>T