Canonical Allele Identifier: PA1139689752
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 887255
ClinVar RCV Id: RCV001119887 RCV001119888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ile541Val
CA7294500
NM_000369.2:c.1621A>G