Canonical Allele Identifier: PA2827016441
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503018

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala1498Val
CA394314530
NM_001318831.2:c.4493C>T