Canonical Allele Identifier: PA2828094069
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1324Lys
CA050575
NM_001363528.2:c.3970G>A