Canonical Allele Identifier: PA2825665081
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 619919
ClinVar RCV Id: RCV000760091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121648.1:p.Leu456Ser
CA351886479
NM_001128176.3:c.1367T>C