Canonical Allele Identifier: PA2580113631
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2237467
ClinVar RCV Id: RCV002724042
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Val724Phe
CA7294597
NM_000369.2:c.2170G>T