Canonical Allele Identifier: PA645463126
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 225506
ClinVar RCV Id: RCV000490322 RCV001118245 RCV001753637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Gly245Ser
CA7294314
NM_000369.2:c.733G>A