ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA111675
Gene: THRB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12551
ClinVar RCV Id:
RCV000013378
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000452.2:p.Lys443Glu
CA122483
NM_000461.5:c.1327A>G