Canonical Allele Identifier: PA2827005971
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468024

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Leu70Arg
CA394306574
NM_001318829.2:c.209T>G