Canonical Allele Identifier: PA2825575266
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073716
ClinVar RCV Id: RCV004016722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys1058Glu
CA394285456
NM_001114382.3:c.3172A>G