Allele Registry

Canonical Allele Identifier: PA118271

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006828

ClinVar Variation:

6457

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Gly431Ser	CA118269 NM_000369.2:c.1291G>A