Canonical Allele Identifier: PA2827926240
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Arg407Cys
CA71604941
NM_001354714.2:c.1219C>T