Canonical Allele Identifier: PA2825577567
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2416226

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Tyr1713Cys
CA394314314
NM_001114382.3:c.5138A>G