Canonical Allele Identifier: PA2825439591
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gln1685Arg
CA394314795
NM_001077183.3:c.5054A>G