Canonical Allele Identifier: PA2827013183
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val479Met
CA035939
NM_001318831.2:c.1435G>A