Canonical Allele Identifier: PA658722278
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12553
ClinVar RCV Id: RCV000013380 RCV000622278 RCV000760097
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Arg320His
CA122487
NM_001252634.2:c.959G>A