Canonical Allele Identifier: PA2825577633
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535883

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gln1729Glu
CA394314782
NM_001114382.3:c.5185C>G