Canonical Allele Identifier: PA915979833
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 314690
ClinVar RCV Id: RCV000284776 RCV000374577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001136098.1:p.Ser53Arg
CA10646433
NM_001142626.3:c.157A>C
CA390770753
NM_001142626.3:c.159T>A
CA390770754
NM_001142626.3:c.159T>G