Allele Registry

Canonical Allele Identifier: PA118208

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006805

RCV001815162

RCV002490329

RCV003466821

ClinVar Variation:

6435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Pro162Ala	CA118206 NM_000369.2:c.484C>G