Canonical Allele Identifier: PA915979835
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 437071
ClinVar RCV Id: RCV000504179 RCV001005031 RCV001223345 RCV001255029 RCV000989248 RCV002524319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Pro68Ser
CA7294029
NM_001142626.3:c.202C>T