Canonical Allele Identifier: PA2828334002
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5212
ClinVar RCV Id: RCV000005522 RCV001753404
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356435.1:p.Gln230Lys
CA117340
NM_001369506.1:c.688C>A