Allele Registry

Canonical Allele Identifier: PA118199

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006801

ClinVar Variation:

6432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Ala623Ile	CA118197 NM_000369.2:c.1867_1868delinsAT