Allele Registry

Canonical Allele Identifier: PA2826353914

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013371

ClinVar Variation:

12544

HGVS (amino-acid)	Matching Registered Transcripts
NP_001239563.1:p.Gly345Asp	CA122471 NM_001252634.2:c.1034G>A