Allele Registry

Canonical Allele Identifier: PA118265

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006826

ClinVar Variation:

6455

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Thr477Ile	CA118263 NM_000369.2:c.1430C>T