Canonical Allele Identifier: PA2827926396
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12550
ClinVar RCV Id: RCV000013377 RCV000725589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Pro422Thr
CA122481
NM_001354715.2:c.1264C>A