Canonical Allele Identifier: PA2825322106
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 623326
ClinVar RCV Id: RCV000761466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018046.1:p.Pro162Ser
CA390734741
NM_001018036.3:c.484C>T