Canonical Allele Identifier: PA2828415541
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2847716
ClinVar RCV Id: RCV003628500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ala1698Gly
CA394314523
NM_001370404.1:c.5093C>G