Canonical Allele Identifier: PA2826169122
Gene: THRA HGNC NCBI

Linked Data

ClinVar Variation Id: 803389
ClinVar RCV Id: RCV000989846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177848.1:p.Arg142Leu
CA399269635
NM_001190919.2:c.425G>T