Allele Registry

Canonical Allele Identifier: PA118259

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006824

ClinVar Variation:

6453

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Lys183Arg	CA118257 NM_000369.2:c.548A>G