Canonical Allele Identifier: PA913197098
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 623326
ClinVar RCV Id: RCV000761466
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Pro162Ser
CA390734741
NM_000369.2:c.484C>T