Canonical Allele Identifier: PA2741838213
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3053994
ClinVar RCV Id: RCV004545718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Asp160Glu
CA7294161
NM_001142626.3:c.480C>A
CA390734720
NM_001142626.3:c.480C>G