Canonical Allele Identifier: PA162654
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 135401
ClinVar RCV Id: RCV000122255 RCV001121768 RCV000954542 RCV001121767 RCV004530043
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg310His
CA162652
NM_000369.2:c.929G>A