Allele Registry

Canonical Allele Identifier: PA2827926212

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013373

ClinVar Variation:

12546

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341643.1:p.Gly316Glu	CA122475 NM_001354714.2:c.947G>A