Canonical Allele Identifier: PA2573065895
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1303494
ClinVar RCV Id: RCV001762952
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Leu471Pro
CA397990728
NM_001139.3:c.1412T>C