Canonical Allele Identifier: PA2827926258
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2442325
ClinVar RCV Id: RCV003149098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Pro422Asn
CA2580069619
NM_001354714.2:c.1264_1265delinsAA