Canonical Allele Identifier: PA658722233
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492909
ClinVar RCV Id: RCV000582505

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Glu227_Thr232dup