Canonical Allele Identifier: PA111554
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12559
ClinVar RCV Id: RCV000013387 RCV001800292 RCV003148621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Arg438His
CA122497
NM_000461.5:c.1313G>A