Canonical Allele Identifier: PA916039265
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492919
ClinVar RCV Id: RCV000583540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Gly345Cys
CA351888714
NM_001354713.2:c.1033G>T