Canonical Allele Identifier: PA2829973417
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207716
ClinVar RCV Id: RCV000189981 RCV001857664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu493Phe
CA319444
NM_021055.3:c.1477C>T