Canonical Allele Identifier: PA104320
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 212729
ClinVar RCV Id: RCV000193750 RCV000421593
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Val527Met
CA277196
NM_001139.3:c.1579G>A