Canonical Allele Identifier: PA162648
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 135399
ClinVar RCV Id: RCV000122253 RCV000299331 RCV000356472 RCV000873340
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Val721Phe
CA162646
NM_000369.2:c.2161G>T