Canonical Allele Identifier: PA1139691017
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 886125
ClinVar RCV Id: RCV001118136 RCV001118137 RCV001593281 RCV002249730 RCV002556512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Glu34Lys
CA7293987
NM_001142626.3:c.100G>A