Canonical Allele Identifier: PA2825574457
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala772Val
CA038376
NM_001114382.3:c.2315C>T