Canonical Allele Identifier: PA2828415584
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gln1708Arg
CA394314795
NM_001370404.1:c.5123A>G