Canonical Allele Identifier: PA2827925816
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341640.1:p.Arg243Gln
CA122509
NM_001354711.2:c.728G>A