Canonical Allele Identifier: PA2826353982
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12561
ClinVar RCV Id: RCV000013389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Phe459Cys
CA122499
NM_001252634.2:c.1376T>G