Allele Registry

Canonical Allele Identifier: PA2826820055

Gene: TAB2 HGNC NCBI

ClinVar RCV:

RCV000005521

ClinVar Variation:

5211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278964.1:p.Pro176Ser	CA117338 NM_001292035.3:c.526C>T