Canonical Allele Identifier: PA118235
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Cys390Trp
CA118233
NM_000369.2:c.1170T>G