Canonical Allele Identifier: PA2827926064
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12564
ClinVar RCV Id: RCV000986043 RCV000852377
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341641.1:p.Val458Ala
CA122505
NM_001354712.2:c.1373T>C