Canonical Allele Identifier: PA2825576820
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509011
ClinVar RCV Id: RCV002016530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile1514Ser
CA394304696
NM_001114382.3:c.4541T>G