Canonical Allele Identifier: PA645463064
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 420145

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Gln90Pro
CA7294058
NM_000369.2:c.269A>C
CA16619887
NM_000369.2:c.267_270delinsTCCT