ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA658722246
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_001239563.1:p.Arg243Gln
CA122509
NM_001252634.2:c.728G>A