Canonical Allele Identifier: PA2827004768
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65095
ClinVar RCV Id: RCV000055306 RCV003512006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1445Pro
CA020803
NM_001318827.2:c.4334T>C