Canonical Allele Identifier: PA916039230
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12566
ClinVar RCV Id: RCV000013394 RCV000760093 RCV002476959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Arg243Gln
CA122509
NM_001354713.2:c.728G>A