Canonical Allele Identifier: PA2829356245
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2043522
ClinVar RCV Id: RCV002895837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002076.2:p.Lys167Arg
CA402939269
NM_002085.4:c.500A>G