Allele Registry

Canonical Allele Identifier: PA118247

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006819

ClinVar Variation:

6449

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Cys672Tyr	CA118245 NM_000369.2:c.2015G>A