Canonical Allele Identifier: PA658722313
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Arg438His
CA122497
NM_001252634.2:c.1313G>A