Canonical Allele Identifier: PA2827925635
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341638.1:p.Val458Ala
CA122505
NM_001354709.2:c.1373T>C