Allele Registry

Canonical Allele Identifier: PA111617

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013372

RCV000986042

ClinVar Variation:

12545

HGVS (amino-acid)	Matching Registered Transcripts
NP_000452.2:p.Gly345Val	CA122473 NM_000461.5:c.1034G>T