Canonical Allele Identifier: PA2827004655
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014334
ClinVar RCV Id: RCV001313056 RCV003166783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ile1415Met
CA394303015
NM_001318827.2:c.4245C>G