Allele Registry

Canonical Allele Identifier: PA2580414818

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV002793873

ClinVar Variation:

2268491

HGVS (amino-acid)	Matching Registered Transcripts
NP_058650.1:p.Glu56Gln	CA413739501 NM_016954.2:c.166G>C