Allele Registry

Canonical Allele Identifier: PA122482

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013377

RCV000725589

ClinVar Variation:

12550

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121649.1:p.Pro453Thr	CA122481 NM_001128177.2:c.1357C>A