Canonical Allele Identifier: PA2825440316
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val645Phe
CA034596
NM_001077183.3:c.1933G>T