Canonical Allele Identifier: PA2829983678
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1706Gln
CA394314713
NM_021055.3:c.5117G>A