Canonical Allele Identifier: PA2825574757
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala862Thr
CA017691
NM_001114382.3:c.2584G>A