Canonical Allele Identifier: PA111572
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12563
ClinVar RCV Id: RCV000013391 RCV003233068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Cys446Arg
CA122503
NM_000461.5:c.1336T>C