Canonical Allele Identifier: PA118268
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6456
ClinVar RCV Id: RCV000006827 RCV000122250 RCV003151707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg310Cys
CA118266
NM_000369.2:c.928C>T