Canonical Allele Identifier: PA118214
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV000006807
ClinVar Variation:
6437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Asp633His
CA118212
NM_000369.2:c.1897G>C