Canonical Allele Identifier: PA2741816280
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2572312
ClinVar RCV Id: RCV003314197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Asp403Asn
CA7294409
NM_000369.2:c.1207G>A