Canonical Allele Identifier: PA1139689704
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 886191
ClinVar RCV Id: RCV001118250 RCV001119783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ile253Thr
CA390725618
NM_000369.2:c.758T>C