Canonical Allele Identifier: PA104157
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 265039
ClinVar RCV Id: RCV000255637 RCV001289939 RCV003155138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Ala597Glu
CA8367177
NM_001139.3:c.1790C>A