Canonical Allele Identifier: PA2826820061
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_001278964.1:p.Gln198Lys
CA117340
NM_001292035.3:c.592C>A