Canonical Allele Identifier: PA2825574885
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016670
ClinVar RCV Id: RCV001315705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg901Leu
CA394279443
NM_001114382.3:c.2702G>T