Canonical Allele Identifier: PA117341
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_055908.1:p.Gln230Lys
CA117340
NM_015093.6:c.688C>A