Canonical Allele Identifier: PA111675
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12551
ClinVar RCV Id: RCV000013378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Lys443Glu
CA122483
NM_000461.5:c.1327A>G