Canonical Allele Identifier: PA916039279
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492921
ClinVar RCV Id: RCV000584262 RCV002469212 RCV003389056 RCV003392424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Arg438Cys
CA71604941
NM_001354713.2:c.1312C>T