Canonical Allele Identifier: PA2828420597
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535857
ClinVar RCV Id: RCV000644067 RCV002256435 RCV003153783
ClinVar Variation Id: 1057663
ClinVar RCV Id: RCV001366691 RCV003155402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser1411Arg
CA394301651
NM_001370405.1:c.4231A>C
CA394301677
NM_001370405.1:c.4233T>A
CA394301688
NM_001370405.1:c.4233T>G