Allele Registry

Canonical Allele Identifier: PA118241

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006816

ClinVar Variation:

6446

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Ser281Ile	CA118239 NM_000369.2:c.842G>T