Canonical Allele Identifier: PA2829970234
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 572351
ClinVar RCV Id: RCV000693713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg29Lys
CA394301347
NM_021055.3:c.86G>A