Canonical Allele Identifier: PA2825436112
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu663Arg
CA394274401
NM_001077183.3:c.1988T>G