Canonical Allele Identifier: PA645463260
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 314698
ClinVar RCV Id: RCV000334617 RCV000401092 RCV003401322
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg707Gln
CA7294588
NM_000369.2:c.2120G>A