Allele Registry

Canonical Allele Identifier: PA118238

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006815

RCV000314691

RCV002512853

RCV003764533

RCV004532302

ClinVar Variation:

6445

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Ala553Thr	CA118236 NM_000369.2:c.1657G>A