Canonical Allele Identifier: PA2827004658
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_001305756.1:p.Leu1416Pro
CA394303025
NM_001318827.2:c.4247T>C