Canonical Allele Identifier: PA2827005507
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Leu1641Val
CA394314564
NM_001318827.2:c.4921C>G