Allele Registry

Canonical Allele Identifier: PA658813978

Gene: IL12B HGNC NCBI

ClinVar RCV:

RCV000652142

ClinVar Variation:

541813

HGVS (amino-acid)	Matching Registered Transcripts
NP_002178.2:p.Gly182Arg	CA3538765 NM_002187.3:c.544G>A CA362032924 NM_002187.3:c.544G>C