Allele Registry

Canonical Allele Identifier: PA916056603

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000213113

RCV000537615

ClinVar Variation:

230395

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser6Asn	CA033570 NM_021055.3:c.17G>A