Canonical Allele Identifier: PA122468
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12542
ClinVar RCV Id: RCV000013369 RCV000760096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Ala317Thr
CA122467
NM_001128177.2:c.949G>A