Canonical Allele Identifier: PA645294985
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 388812
ClinVar RCV Id: RCV000431667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Ser636Ile
CA16607532
NM_001139.3:c.1907G>T