Canonical Allele Identifier: PA128762
Gene: THRA HGNC NCBI

Linked Data

ClinVar Variation Id: 29913
ClinVar RCV Id: RCV000022800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003241.2:p.Ser45Ile
CA128759
NM_003250.5:c.134G>T