Allele Registry

Canonical Allele Identifier: PA122476

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013373

ClinVar Variation:

12546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121649.1:p.Gly347Glu	CA122475 NM_001128177.2:c.1040G>A