Canonical Allele Identifier: PA2825434687
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu219Pro
CA022749
NM_001077183.3:c.656T>C