Canonical Allele Identifier: PA2825440393
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val766Ala
CA038262
NM_001077183.3:c.2297T>C