Canonical Allele Identifier: PA2827008308
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu908Met
CA394283761
NM_001318829.2:c.2722T>A