Canonical Allele Identifier: PA2825396369
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722592
ClinVar RCV Id: RCV002305702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035810.1:p.Val284Ala
CA415235091
NM_001042351.2:c.851T>C