ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827925921
Gene: THRB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12564
ClinVar RCV Id:
RCV000986043
RCV000852377
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341640.1:p.Val458Ala
CA122505
NM_001354711.2:c.1373T>C