Allele Registry

Canonical Allele Identifier: PA118256

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006823

ClinVar Variation:

6452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Ser281Asn	CA118254 NM_000369.2:c.842G>A