Canonical Allele Identifier: PA1139689723
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 886255
ClinVar RCV Id: RCV001118350 RCV001118351 RCV002245863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg519His
CA7294480
NM_000369.2:c.1556G>A