Canonical Allele Identifier: PA2573175569
Gene: GPX4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365138
ClinVar RCV Id: RCV001929715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034937.1:p.Ala197Thr
CA303994421
NM_001039848.4:c.589G>A