Allele Registry

Canonical Allele Identifier: PA2829981482

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000546695

ClinVar Variation:

468092

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Gln1460Arg	CA394302741 NM_021055.3:c.4379A>G