Canonical Allele Identifier: PA2825146274
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Arg438Cys
CA71604941
NM_000461.5:c.1312C>T