Canonical Allele Identifier: PA2580135585
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2043522
ClinVar RCV Id: RCV002895837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034937.1:p.Lys204Arg
CA402939269
NM_001039848.4:c.611A>G