Allele Registry

Canonical Allele Identifier: PA2741938315

Gene: TBX21 HGNC NCBI

ClinVar RCV:

RCV003489229

ClinVar Variation:

2688320

HGVS (amino-acid)	Matching Registered Transcripts
NP_037483.1:p.His33Gln	CA8626238 NM_013351.2:c.99C>G CA400057599 NM_013351.2:c.99C>A