Canonical Allele Identifier: PA2825158518
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3183663
ClinVar RCV Id: RCV004476480
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Phe355Ser
CA390726584
NM_000369.2:c.1064T>C