Canonical Allele Identifier: PA2827925753
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492921

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341639.1:p.Arg438Cys
CA71604941
NM_001354710.2:c.1312C>T