Canonical Allele Identifier: PA162651
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 135400
ClinVar RCV Id: RCV000122254 RCV000302729 RCV000392451 RCV001541679 RCV001839917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Glu727Asp
CA162649
NM_000369.2:c.2181G>C
CA390729655
NM_000369.2:c.2181G>T