Canonical Allele Identifier: PA915979858
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV000006824
ClinVar Variation:
6453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Lys183Arg
CA118257
NM_001142626.3:c.548A>G