Canonical Allele Identifier: PA2825187477
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232170
ClinVar RCV Id: RCV004520853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Ile1518Leu
CA394303004
NM_000548.5:c.4552A>C