Canonical Allele Identifier: PA128761
Gene: THRA HGNC NCBI

Linked Data

ClinVar Variation Id: 29913
ClinVar RCV Id: RCV000022800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177848.1:p.Ser45Ile
CA128759
NM_001190919.2:c.134G>T