Canonical Allele Identifier: PA2580111136
Gene: G6PD HGNC NCBI

Linked Data

ClinVar Variation Id: 1722689
ClinVar RCV Id: RCV002305799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000393.4:p.Pro519Leu
CA415232133
NM_000402.4:c.1556C>T