Canonical Allele Identifier: PA2825665028
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12535
ClinVar RCV Id: RCV000013362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121648.1:p.Gly345Arg
CA122452
NM_001128176.3:c.1033G>C