Canonical Allele Identifier: PA645294967
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 325916
ClinVar RCV Id: RCV000280497 RCV003765890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Ala101Thr
CA8367715
NM_001139.3:c.301G>A