Canonical Allele Identifier: PA2825435032
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu332Lys
CA276776600
NM_001077183.3:c.994G>A