Canonical Allele Identifier: PA2827005014
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2827016
ClinVar RCV Id: RCV003628131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val1515Leu
CA394308223
NM_001318827.2:c.4543G>C