Allele Registry

Canonical Allele Identifier: PA2829858130

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012087

ClinVar Variation:

11334

HGVS (amino-acid)	Matching Registered Transcripts
NP_058650.1:p.Leu214Pro	CA121427 NM_016954.2:c.641T>C