Canonical Allele Identifier: PA916062606
Gene: THRA HGNC NCBI

Linked Data

ClinVar Variation Id: 803389
ClinVar RCV Id: RCV000989846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_955366.1:p.Arg142Leu
CA399269635
NM_199334.5:c.425G>T