Canonical Allele Identifier: PA645294984
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 374101
ClinVar RCV Id: RCV000414766 RCV001289513
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Amino-acid Alleles

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