Canonical Allele Identifier: PA2825322093
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018046.1:p.Arg109Gln
CA118215
NM_001018036.3:c.326G>A