Canonical Allele Identifier: PA2828413085
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728211
ClinVar RCV Id: RCV002320843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu1007Arg
CA394285304
NM_001370404.1:c.3020T>G