Canonical Allele Identifier: PA915979832
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 135392
ClinVar RCV Id: RCV000122244 RCV000319857 RCV001118138 RCV001657769 RCV001839916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Pro52Thr
CA248749
NM_001142626.3:c.154C>A