Canonical Allele Identifier: PA2827014985
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Glu1100Lys
CA050233
NM_001318831.2:c.3298G>A