Canonical Allele Identifier: PA2827005538
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gln1649Arg
CA394314795
NM_001318827.2:c.4946A>G