Allele Registry

Canonical Allele Identifier: PA2828204598

Gene: TBXT HGNC NCBI

ClinVar RCV:

RCV001641636

RCV001815598

ClinVar Variation:

1242832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001353215.1:p.Gly177Asp	CA4093060 NM_001366286.2:c.530G>A