Canonical Allele Identifier: PA1139685307
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 995500
ClinVar RCV Id: RCV001289534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001130.1:p.Phe99Leu
CA397999187
NM_001139.3:c.297C>G
CA397999189
NM_001139.3:c.297C>A
CA397999209
NM_001139.3:c.295T>C