Allele Registry

Canonical Allele Identifier: PA915979822

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006799

RCV000122245

RCV000259846

RCV000373195

RCV000870612

ClinVar Variation:

6430

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Asp36His	CA118191 NM_001142626.3:c.106G>C