Canonical Allele Identifier: PA2826353978
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Val458Ala
CA122505
NM_001252634.2:c.1373T>C