Canonical Allele Identifier: PA2580150138
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 2408923
ClinVar RCV Id: RCV002764841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Ile96Thr
CA8367717
NM_001139.3:c.287T>C