Canonical Allele Identifier: PA1139689710
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 887199
ClinVar RCV Id: RCV001119788 RCV001121766 RCV002556560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ser305Arg
CA7294360
NM_000369.2:c.915T>A
CA390726238
NM_000369.2:c.913A>C
CA390726243
NM_000369.2:c.915T>G