Canonical Allele Identifier: PA2827007464
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406765
ClinVar RCV Id: RCV001915976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gly605Arg
CA394273606
NM_001318829.2:c.1813G>C