Canonical Allele Identifier: PA915979847
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_001136098.1:p.Pro162Ser
CA390734741
NM_001142626.3:c.484C>T