Allele Registry

Canonical Allele Identifier: PA122514

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013396

ClinVar Variation:

12568

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121649.1:p.Arg383His	CA122513 NM_001128177.2:c.1148G>A