Canonical Allele Identifier: PA1139689762
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 886325
ClinVar RCV Id: RCV001118460 RCV001118461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Gly753Ser
CA7294614
NM_000369.2:c.2257G>A