Allele Registry

Canonical Allele Identifier: PA2825556519

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012082

ClinVar Variation:

11329

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103349.1:p.Thr140Met	CA121423 NM_001109879.2:c.419C>T