Allele Registry

Canonical Allele Identifier: PA2825322116

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006824

ClinVar Variation:

6453

HGVS (amino-acid)	Matching Registered Transcripts
NP_001018046.1:p.Lys183Arg	CA118257 NM_001018036.3:c.548A>G