Allele Registry

Canonical Allele Identifier: PA915979847

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000761466

ClinVar Variation:

623326

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Pro162Ser	CA390734741 NM_001142626.3:c.484C>T