Canonical Allele Identifier: PA2827002076
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2178101
ClinVar RCV Id: RCV002588518 RCV004068834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val642Ala
CA394274557
NM_001318827.2:c.1925T>C