Canonical Allele Identifier: PA118229
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 6442
ClinVar RCV Id: RCV000006812 RCV000415318 RCV001197388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Cys41Ser
CA118227
NM_000369.2:c.122G>C
CA390770674
NM_000369.2:c.121T>A