Canonical Allele Identifier: PA2827003684
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392807
ClinVar RCV Id: RCV001912404 RCV002458744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser1140Phe
CA394292073
NM_001318827.2:c.3419C>T