Canonical Allele Identifier: PA2825437564
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1117Val
CA019204
NM_001077183.3:c.3350C>T