Canonical Allele Identifier: PA2825158430
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 3053994
ClinVar RCV Id: RCV004545718
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Asp160Glu
CA7294161
NM_000369.2:c.480C>A
CA390734720
NM_000369.2:c.480C>G