Canonical Allele Identifier: PA2580150149
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1949169
ClinVar RCV Id: RCV002676051
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Gly459Ser
CA8367319
NM_001139.3:c.1375G>A