Allele Registry

Canonical Allele Identifier: PA118226

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006811

ClinVar Variation:

6441

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Asp410Asn	CA118224 NM_000369.2:c.1228G>A