Canonical Allele Identifier: PA2580272718
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 2162141
ClinVar RCV Id: RCV003070091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002178.2:p.Pro39Ala
CA3538879
NM_002187.3:c.115C>G