Canonical Allele Identifier: PA2827011701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val119Met
CA394315689
NM_001318831.2:c.355G>A