Canonical Allele Identifier: PA2827002832
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2037148
ClinVar RCV Id: RCV002885537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Cys863Arg
CA394279428
NM_001318827.2:c.2587T>C