Allele Registry

Canonical Allele Identifier: PA111727

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000507528

RCV000583070

ClinVar Variation:

439310

HGVS (amino-acid)	Matching Registered Transcripts
NP_000452.2:p.Pro453Ser	CA351886499 NM_000461.5:c.1357C>T