Allele Registry

Canonical Allele Identifier: PA118232

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006813

ClinVar Variation:

6443

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Phe525Leu	CA118230 NM_000369.2:c.1575C>A CA390728175 NM_000369.2:c.1573T>C CA390728179 NM_000369.2:c.1575C>G