Canonical Allele Identifier: PA645463204
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 418666
ClinVar RCV Id: RCV000487167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ser508Leu
CA7294468
NM_000369.2:c.1523C>T