Canonical Allele Identifier: PA916023107
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu935Lys
CA019256
NM_001318831.2:c.2803G>A