Allele Registry

Canonical Allele Identifier: PA118211

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000006806

ClinVar Variation:

6436

HGVS (amino-acid)	Matching Registered Transcripts
NP_000360.2:p.Met453Thr	CA118209 NM_000369.2:c.1358T>C CA645584899 NM_000369.2:c.1358_1359delinsCC