Canonical Allele Identifier: PA1139689758
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 917861
ClinVar RCV Id: RCV001175135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ile654Phe
CA7294554
NM_000369.2:c.1960A>T