Allele Registry

Canonical Allele Identifier: PA100338

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012087

ClinVar Variation:

11334

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103348.1:p.Leu214Pro	CA121427 NM_001109878.2:c.641T>C