Allele Registry

Canonical Allele Identifier: PA916019614

Gene: TBX22 HGNC NCBI

ClinVar RCV:

RCV000012087

ClinVar Variation:

11334

HGVS (amino-acid)	Matching Registered Transcripts
NP_001290404.1:p.Leu94Pro	CA121427 NM_001303475.1:c.281T>C