Canonical Allele Identifier: PA2825574687
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232117
ClinVar RCV Id: RCV004520800

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro842Ala
CA394277939
NM_001114382.3:c.2524C>G