Allele Registry

Canonical Allele Identifier: PA2827001330

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001011553

ClinVar Variation:

819200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Gln441Glu	CA394324088 NM_001318827.2:c.1321C>G