Canonical Allele Identifier: PA2827926205
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_001341643.1:p.Gly313Glu
CA351888716
NM_001354714.2:c.938G>A