Allele Registry

Canonical Allele Identifier: PA645393375

Gene: ALOX12B HGNC NCBI

ClinVar RCV:

RCV000498313

ClinVar Variation:

432898

HGVS (amino-acid)	Matching Registered Transcripts
NP_001130.1:p.Pro620Leu	CA397986241 NM_001139.3:c.1859C>T