Canonical Allele Identifier: PA658681251
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468100
ClinVar RCV Id: RCV000537005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1519Pro
CA394303025
NM_000548.5:c.4556T>C