Canonical Allele Identifier: PA2827009463
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1327Lys
CA020286
NM_001318829.2:c.3979G>A