Canonical Allele Identifier: PA2827925385
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12566
ClinVar RCV Id: RCV000013394 RCV000760093 RCV002476959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341637.1:p.Arg243Gln
CA122509
NM_001354708.2:c.728G>A