Canonical Allele Identifier: PA2825322113
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2544142
ClinVar RCV Id: RCV003272354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018046.1:p.Leu175Val
CA390734915
NM_001018036.3:c.523C>G