Canonical Allele Identifier: PA118250
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ser505Asn
CA118248
NM_000369.2:c.1514G>A