Canonical Allele Identifier: PA2829982066
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu1535Pro
CA020960
NM_021055.3:c.4604T>C