Allele Registry

Canonical Allele Identifier: PA2827926209

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013371

ClinVar Variation:

12544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341643.1:p.Gly314Asp	CA122471 NM_001354714.2:c.941G>A