Canonical Allele Identifier: PA2827021021
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1701Lys
CA16615048
NM_001318832.2:c.5101G>A