Allele Registry

Canonical Allele Identifier: PA118262

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006825

ClinVar Variation:

6454

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Pro639Ser	CA118260 NM_000369.2:c.1915C>T