Allele Registry

Canonical Allele Identifier: PA915979854

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006805

RCV001815162

RCV002490329

RCV003466821

ClinVar Variation:

6435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Pro162Ala	CA118206 NM_001142626.3:c.484C>G