Canonical Allele Identifier: PA2825436586
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Cys804Arg
CA017384
NM_001077183.3:c.2410T>C