Canonical Allele Identifier: PA093097
Gene: TAB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 5212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001278963.1:p.Gln230Lys
CA117340
NM_001292034.3:c.688C>A