Canonical Allele Identifier: PA2828414701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232170
ClinVar RCV Id: RCV004520853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile1474Leu
CA394303004
NM_001370404.1:c.4420A>C