Canonical Allele Identifier: PA2827925756
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12551
ClinVar RCV Id: RCV000013378
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341639.1:p.Lys443Glu
CA122483
NM_001354710.2:c.1327A>G