Canonical Allele Identifier: PA2827010452
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1634Gln
CA394314713
NM_001318829.2:c.4901G>A