Allele Registry

Canonical Allele Identifier: PA100331

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012083

ClinVar Variation:

11330

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103348.1:p.Gly118Cys	CA121424 NM_001109878.2:c.352G>T