Allele Registry

Canonical Allele Identifier: PA2827004367

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV002716230

ClinVar Variation:

1963872

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Glu1339Gln	CA394301341 NM_001318827.2:c.4015G>C