Canonical Allele Identifier: PA2828274800
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1514972
ClinVar RCV Id: RCV002029696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001354761.1:p.Asp144Gly
CA9037467
NM_001367832.1:c.431A>G