Canonical Allele Identifier: PA2825439579
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1682Gln
CA394314713
NM_001077183.3:c.5045G>A