Allele Registry

Canonical Allele Identifier: PA117339

Gene: TAB2 HGNC NCBI

ClinVar RCV:

RCV000005521

ClinVar Variation:

5211

HGVS (amino-acid)	Matching Registered Transcripts
NP_055908.1:p.Pro208Ser	CA117338 NM_015093.6:c.622C>T