Allele Registry

Canonical Allele Identifier: PA916039292

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000584309

RCV001284714

ClinVar Variation:

492924

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341642.1:p.Pro453Ala	CA2287079 NM_001354713.2:c.1357C>G