Canonical Allele Identifier: PA2825665109
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492909
ClinVar RCV Id: RCV000582505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Glu227_Thr232dup
CA658683301
NM_001128177.2:c.679_696dup