Canonical Allele Identifier: PA2827010428
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721813
ClinVar RCV Id: RCV002295049

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu1629Val
CA394314564
NM_001318829.2:c.4885C>G