Canonical Allele Identifier: PA2825438044
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 448730

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly1258Asp
CA049827
NM_001077183.3:c.3773G>A