Canonical Allele Identifier: PA2827020984
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1693Gln
CA394314713
NM_001318832.2:c.5078G>A