Canonical Allele Identifier: PA2825158443
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2544142
ClinVar RCV Id: RCV003272354
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Leu175Val
CA390734915
NM_000369.2:c.523C>G