Allele Registry

Canonical Allele Identifier: PA915979856

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006804

ClinVar Variation:

6434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Ile167Asn	CA118203 NM_001142626.3:c.500T>A