Canonical Allele Identifier: PA2825439307
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1612Lys
CA021570
NM_001077183.3:c.4834G>A