Canonical Allele Identifier: PA2825575242
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 936312
ClinVar RCV Id: RCV001205088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1049Gln
CA394285219
NM_001114382.3:c.3145G>C