Canonical Allele Identifier: PA118259
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV000006824
ClinVar Variation:
6453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Lys183Arg
CA118257
NM_000369.2:c.548A>G