Allele Registry

Canonical Allele Identifier: PA118202

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006802

RCV000006803

ClinVar Variation:

6433

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Phe631Leu	CA118200 NM_000369.2:c.1891T>C CA390728848 NM_000369.2:c.1893C>A CA390728849 NM_000369.2:c.1893C>G