Canonical Allele Identifier: PA2829983293
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039113
ClinVar RCV Id: RCV001342520 RCV003238861
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Ala1673Val
CA394312611
NM_021055.3:c.5018C>T