Canonical Allele Identifier: PA2580110777
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722759
ClinVar RCV Id: RCV002305869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Val301Leu
CA415235270
NM_000402.4:c.901G>T
CA415235272
NM_000402.4:c.901G>C