Canonical Allele Identifier: PA2829978299
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1024Leu
CA044723
NM_021055.3:c.3070G>C