Canonical Allele Identifier: PA2825435619
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu528Pro
CA015160
NM_001077183.3:c.1583T>C