Canonical Allele Identifier: PA2827016490
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2814113
ClinVar RCV Id: RCV003627868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1509Gly
CA394314811
NM_001318831.2:c.4525C>G