Canonical Allele Identifier: PA2829979563
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040960
ClinVar RCV Id: RCV001344698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1188Pro
CA394292479
NM_021055.3:c.3563T>C