Allele Registry

Canonical Allele Identifier: PA100322

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012089

ClinVar Variation:

11336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103348.1:p.Asn264Tyr	CA121428 NM_001109878.2:c.790A>T