Canonical Allele Identifier: PA2827926267
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12561
ClinVar RCV Id: RCV000013389
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Phe428Cys
CA122499
NM_001354714.2:c.1283T>G