Canonical Allele Identifier: PA2499260637
Gene: IL12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1018823
ClinVar RCV Id: RCV001318179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002178.2:p.Val212Leu
CA362032532
NM_002187.3:c.634G>C
CA362032534
NM_002187.3:c.634G>T