Canonical Allele Identifier: PA104311
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 39546
ClinVar RCV Id: RCV000032744 RCV000413764 RCV000414880 RCV002222361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Tyr521Cys
CA261173
NM_001139.3:c.1562A>G