Canonical Allele Identifier: PA2829984378
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_066399.2:p.Glu1758Asp
CA16615209
NM_021055.3:c.5274G>T
CA394316180
NM_021055.3:c.5274G>C