Canonical Allele Identifier: PA204913
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 208788
ClinVar RCV Id: RCV000190814 RCV001115207 RCV001118346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Val448Ile
CA204911
NM_000369.2:c.1342G>A