Canonical Allele Identifier: PA2829356249
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_002076.2:p.Asp171Gly
CA9037467
NM_002085.4:c.512A>G