Canonical Allele Identifier: PA1139685312
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 995750
ClinVar RCV Id: RCV001289959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Pro100Leu
CA397999160
NM_001139.3:c.299C>T