Canonical Allele Identifier: PA2580135581
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2098375
ClinVar RCV Id: RCV003030918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034937.1:p.Lys199Glu
CA9037416
NM_001039848.4:c.595A>G