Canonical Allele Identifier: PA2827926065
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12561
ClinVar RCV Id: RCV000013389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341641.1:p.Phe459Cys
CA122499
NM_001354712.2:c.1376T>G