Canonical Allele Identifier: PA122486
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12552
ClinVar RCV Id: RCV000013379 RCV002476957
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Gly345Ser
CA122485
NM_001128177.2:c.1033G>A