Canonical Allele Identifier: PA2827926186
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Arg289His
CA122487
NM_001354714.2:c.866G>A