Canonical Allele Identifier: PA2827926374
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Arg407His
CA122497
NM_001354715.2:c.1220G>A