Canonical Allele Identifier: PA2825436475
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala772Val
CA038376
NM_001077183.3:c.2315C>T