Canonical Allele Identifier: PA2825437822
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50015
ClinVar RCV Id: RCV000043283 RCV000537246 RCV003162359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1196Cys
CA019506
NM_001077183.3:c.3586C>T