Allele Registry

Canonical Allele Identifier: PA2826884048

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012089

ClinVar Variation:

11336

HGVS (amino-acid)	Matching Registered Transcripts
NP_001290404.1:p.Asn144Tyr	CA121428 NM_001303475.1:c.430A>T