Canonical Allele Identifier: PA126190
Gene: GPX1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16082
ClinVar RCV Id: RCV000017462 RCV001675582 RCV002496389
JSON-LD

Amino-acid Alleles

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