Canonical Allele Identifier: PA2827926393
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 1683251
ClinVar RCV Id: RCV002238572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Pro422Asp
CA2573136162
NM_001354715.2:c.1264_1265delinsGA