Canonical Allele Identifier: PA891853985
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 570949
ClinVar RCV Id: RCV000691948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002178.2:p.Pro235Ser
CA3538731
NM_002187.3:c.703C>T