Canonical Allele Identifier: PA2827014317
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val823Leu
CA044723
NM_001318831.2:c.2467G>C