Canonical Allele Identifier: PA2825577617
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys1725Thr
CA394314672
NM_001114382.3:c.5174A>C