Allele Registry

Canonical Allele Identifier: PA2828414639

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000546695

ClinVar Variation:

468092

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Gln1459Arg	CA394302741 NM_001370404.1:c.4376A>G