Allele Registry

Canonical Allele Identifier: PA2826884046

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012082

ClinVar Variation:

11329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001290404.1:p.Thr140Met	CA121423 NM_001303475.1:c.419C>T