Canonical Allele Identifier: PA118277
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6459
ClinVar RCV Id: RCV000006830

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Leu467Pro
CA118275
NM_000369.2:c.1400T>C