Canonical Allele Identifier: PA2827009575
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1359Gly
CA051088
NM_001318829.2:c.4075A>G