Canonical Allele Identifier: PA2829974398
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237972
ClinVar RCV Id: RCV000227968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala614Pro
CA10583299
NM_021055.3:c.1840G>C