Canonical Allele Identifier: PA2829983664
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564709
ClinVar RCV Id: RCV003297141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Lys1705Thr
CA394314672
NM_021055.3:c.5114A>C