Canonical Allele Identifier: PA2825439590
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gln1685Glu
CA394314782
NM_001077183.3:c.5053C>G