Canonical Allele Identifier: PA118217
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg109Gln
CA118215
NM_000369.2:c.326G>A