Canonical Allele Identifier: PA2828093361
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ala1118Val
CA019204
NM_001363528.2:c.3353C>T