Canonical Allele Identifier: PA122498
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Arg438His
CA122497
NM_001128177.2:c.1313G>A