Canonical Allele Identifier: PA2828419226
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238013
ClinVar RCV Id: RCV000228906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Leu1009Pro
CA10583318
NM_001370405.1:c.3026T>C