Canonical Allele Identifier: PA2827012892
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Ala407Val
CA015881
NM_001318831.2:c.1220C>T