Canonical Allele Identifier: PA2825665135
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492918
ClinVar RCV Id: RCV000582292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Gly344Glu
CA351888716
NM_001128177.2:c.1031G>A