Allele Registry

Canonical Allele Identifier: PA645463185

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000273881

RCV000490528

RCV000826152

RCV003153491

RCV003225722

ClinVar Variation:

225505

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Arg450His	CA7294442 NM_000369.2:c.1349G>A