Canonical Allele Identifier: PA915979839
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 420145
ClinVar RCV Id: RCV000483426 RCV004541520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Gln90Pro
CA7294058
NM_001142626.3:c.269A>C
CA16619887
NM_001142626.3:c.267_270delinsTCCT