Allele Registry

Canonical Allele Identifier: PA2827926007

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013371

ClinVar Variation:

12544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341641.1:p.Gly345Asp	CA122471 NM_001354712.2:c.1034G>A