Canonical Allele Identifier: PA2828415575
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1705Gln
CA394314713
NM_001370404.1:c.5114G>A