Canonical Allele Identifier: PA095252
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 100057
ClinVar RCV Id: RCV000011087 RCV000079409 RCV000011086 RCV000011088 RCV000179363 RCV000445579 RCV000477810 RCV001250219 RCV000623137 RCV000761429 RCV001265539 RCV002227060 RCV003925095 RCV001528124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035810.1:p.Ser188Phe
CA120955
NM_001042351.2:c.563C>T
CA2580573398
NM_001042351.2:c.[563C>T;376A>G;202G>A]
CA2580573399
NM_001042351.2:c.[563C>T;376A>G]
CA2580573400
NM_001042351.2:c.[563C>T;202G>A]
CA2580573401
NM_001042351.2:c.[563C>T;143T>C]