Canonical Allele Identifier: PA2827016483
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Gln1508Arg
CA394314795
NM_001318831.2:c.4523A>G