Allele Registry

Canonical Allele Identifier: PA126190

Gene: GPX1 HGNC NCBI

ClinVar Allele:

31121

ClinVar RCV:

RCV000017462

RCV001675582

RCV002496389

ClinVar Variation:

16082

HGVS (amino-acid)	Matching Registered Transcripts
NP_000572.2:p.Pro200Leu	CA126189 NM_000581.4:c.599C>T