Canonical Allele Identifier: PA2825322105
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3053994
ClinVar RCV Id: RCV004545718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018046.1:p.Asp160Glu
CA7294161
NM_001018036.3:c.480C>A
CA390734720
NM_001018036.3:c.480C>G