Canonical Allele Identifier: PA2825158502
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3183667
ClinVar RCV Id: RCV004476484
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Arg310Leu
CA263934906
NM_000369.2:c.929G>T