Canonical Allele Identifier: PA2825438478
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468084

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1384Ser
CA050936
NM_001077183.3:c.4150C>A