Allele Registry

Canonical Allele Identifier: PA118244

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006818

ClinVar Variation:

6448

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Val509Ala	CA118242 NM_000369.2:c.1526T>C