Allele Registry

Canonical Allele Identifier: PA100372

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012082

ClinVar Variation:

11329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103348.1:p.Thr260Met	CA121423 NM_001109878.2:c.779C>T