Canonical Allele Identifier: PA2829983703
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gln1709Arg
CA394314795
NM_021055.3:c.5126A>G