Canonical Allele Identifier: PA2825438885
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1491Lys
CA020888
NM_001077183.3:c.4471G>A