ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825322106
Gene: TSHR
HGNC
NCBI
Linked Data
ClinVar Variation Id:
623326
ClinVar RCV Id:
RCV000761466
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001018046.1:p.Pro162Ser
CA390734741
NM_001018036.3:c.484C>T