Canonical Allele Identifier: PA2741816302
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2736136
ClinVar RCV Id: RCV003557831
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg519Cys
CA7294479
NM_000369.2:c.1555C>T