Canonical Allele Identifier: PA2828090924
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 389695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Cys414Gly
CA16608029
NM_001363528.2:c.1240T>G