Canonical Allele Identifier: PA2827004042
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207750

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu1241Lys
CA050233
NM_001318827.2:c.3721G>A