Allele Registry

Canonical Allele Identifier: PA118250

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006820

RCV002468962

ClinVar Variation:

6450

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Ser505Asn	CA118248 NM_000369.2:c.1514G>A