Canonical Allele Identifier: PA658805075
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Glu1360Lys
CA050377
NM_000548.5:c.4078G>A