Canonical Allele Identifier: PA658678297
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 474973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002178.2:p.Val33Ile
CA3538882
NM_002187.3:c.97G>A