Canonical Allele Identifier: PA2827019409
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1265Val
CA019757
NM_001318832.2:c.3794A>T