Canonical Allele Identifier: PA261172
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 39545
ClinVar RCV Id: RCV000032743 RCV000414417 RCV000626762 RCV002509181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Arg548Trp
CA261171
NM_001139.3:c.1642C>T