Canonical Allele Identifier: PA2826169096
Gene: THRA HGNC NCBI

Linked Data

ClinVar Variation Id: 522121
ClinVar RCV Id: RCV000623448 RCV002305517 RCV003129944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177847.1:p.Ala263Val
CA399274760
NM_001190918.2:c.788C>T