Canonical Allele Identifier: PA2825577855
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405970
ClinVar RCV Id: RCV000465811 RCV002348292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1778Asp
CA16615209
NM_001114382.3:c.5334G>T
CA394316180
NM_001114382.3:c.5334G>C