Allele Registry

Canonical Allele Identifier: PA2826353892

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000449629

ClinVar Variation:

397581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001239563.1:p.Glu326Gly	CA16609441 NM_001252634.2:c.977A>G