Allele Registry

Canonical Allele Identifier: PA118235

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006814

RCV002490330

ClinVar Variation:

6444

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Cys390Trp	CA118233 NM_000369.2:c.1170T>G