Canonical Allele Identifier: PA2825438701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1741247
ClinVar RCV Id: RCV002340027
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Phe1443Ser
CA394302858
NM_001077183.3:c.4328T>C