Canonical Allele Identifier: PA2828415610
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu1713Lys
CA16615048
NM_001370404.1:c.5137G>A