Canonical Allele Identifier: PA2826169076
Gene: THRA HGNC NCBI
ClinVar RCV:
RCV002308782
ClinVar Variation:
1723508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177847.1:p.Lys49Arg
CA399265296
NM_001190918.2:c.146A>G