Canonical Allele Identifier: PA2499231798
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 981847
ClinVar RCV Id: RCV001374528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Leu557Trp
CA390728372
NM_000369.2:c.1670T>G