Allele Registry

Canonical Allele Identifier: PA2825571851

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000213113

RCV000537615

ClinVar Variation:

230395

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ser6Asn	CA033570 NM_001114382.3:c.17G>A