Canonical Allele Identifier: PA2828411958
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Pro670Leu
CA016425
NM_001370404.1:c.2009C>T