Allele Registry

Canonical Allele Identifier: PA2827926390

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000507528

RCV000583070

ClinVar Variation:

439310

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341644.1:p.Pro422Ser	CA351886499 NM_001354715.2:c.1264C>T