Allele Registry

Canonical Allele Identifier: PA1139691031

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV001121665

RCV001121666

ClinVar Variation:

888395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Thr136Ala	CA390734300 NM_001142626.3:c.406A>G