Allele Registry

Canonical Allele Identifier: PA118253

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006821

RCV000006822

ClinVar Variation:

6451

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Leu629Phe	CA118251 NM_000369.2:c.1887G>T CA390728835 NM_000369.2:c.1887G>C