Canonical Allele Identifier: PA264677
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65283
ClinVar RCV Id: RCV000055504 RCV000498705 RCV002298458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1066Pro
CA018667
NM_000548.5:c.3197T>C