Allele Registry

Canonical Allele Identifier: PA645294984

Gene: ALOX12B HGNC NCBI

ClinVar RCV:

RCV000414766

RCV001289513

ClinVar Variation:

374101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001130.1:p.Pro620Gln	CA8367165 NM_001139.3:c.1859C>A