Canonical Allele Identifier: PA2827267989
Gene: GPX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2432258
ClinVar RCV Id: RCV003131069

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316431.1:p.Ala18Ser
CA352783647
NM_001329502.2:c.52G>T