ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827926186
Gene: THRB
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12553
ClinVar RCV Id:
RCV000013380
RCV000622278
RCV000760097
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341643.1:p.Arg289His
CA122487
NM_001354714.2:c.866G>A