Canonical Allele Identifier: PA2828411405
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Leu528Pro
CA015160
NM_001370404.1:c.1583T>C