Allele Registry

Canonical Allele Identifier: PA111739

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013377

RCV000725589

ClinVar Variation:

12550

HGVS (amino-acid)	Matching Registered Transcripts
NP_000452.2:p.Pro453Thr	CA122481 NM_000461.5:c.1357C>A