Allele Registry

Canonical Allele Identifier: PA2741816326

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV003317738

ClinVar Variation:

2573402

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Asp633Asn	CA263936324 NM_000369.2:c.1897G>A