Allele Registry

Canonical Allele Identifier: PA2825556454

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV002793873

ClinVar Variation:

2268491

HGVS (amino-acid)	Matching Registered Transcripts
NP_001103348.1:p.Glu56Gln	CA413739501 NM_001109878.2:c.166G>C