Canonical Allele Identifier: PA111609
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12552
ClinVar RCV Id: RCV000013379 RCV002476957
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Gly345Ser
CA122485
NM_000461.5:c.1033G>A