Allele Registry

Canonical Allele Identifier: PA118268

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006827

RCV000122250

RCV003151707

ClinVar Variation:

6456

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Arg310Cys	CA118266 NM_000369.2:c.928C>T