Allele Registry

Canonical Allele Identifier: PA118217

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006808

RCV003555948

ClinVar Variation:

6438

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Arg109Gln	CA118215 NM_000369.2:c.326G>A