Canonical Allele Identifier: PA2827926131
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 1683251
ClinVar RCV Id: RCV002238572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Pro453Asp
CA2573136162
NM_001354713.2:c.1357_1358delinsGA