Canonical Allele Identifier: PA2829983722
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2814113
ClinVar RCV Id: RCV003627868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1710Gly
CA394314811
NM_021055.3:c.5128C>G