Canonical Allele Identifier: PA2825577632
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gln1729Arg
CA394314795
NM_001114382.3:c.5186A>G