Canonical Allele Identifier: PA2827926333
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2573413
ClinVar RCV Id: RCV003317749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Arg307Gln
CA351888757
NM_001354715.2:c.920G>A