Canonical Allele Identifier: PA2829973630
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64901

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu528Pro
CA015160
NM_021055.3:c.1583T>C