Allele Registry

Canonical Allele Identifier: PA2829981009

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV002716230

ClinVar Variation:

1963872

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1399Gln	CA394301341 NM_021055.3:c.4195G>C