Canonical Allele Identifier: PA2825322116
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV000006824
ClinVar Variation:
6453
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001018046.1:p.Lys183Arg
CA118257
NM_001018036.3:c.548A>G