Canonical Allele Identifier: PA2828091605
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1780872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile610Leu
CA394273001
NM_001363528.2:c.1828A>C