Canonical Allele Identifier: PA2828095396
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Lys1682Thr
CA394314672
NM_001363528.2:c.5045A>C