Allele Registry

Canonical Allele Identifier: PA111590

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000013370

RCV000424820

RCV002265554

ClinVar Variation:

12543

HGVS (amino-acid)	Matching Registered Transcripts
NP_000452.2:p.Gly332Arg	CA122469 NM_000461.5:c.994G>A CA351888796 NM_000461.5:c.994G>C