Allele Registry

Canonical Allele Identifier: PA2829978277

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000734482

RCV001019085

RCV001051568

RCV001083071

RCV002258838

RCV003329362

RCV003998821

ClinVar Variation:

238014

823131

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Asn1021Lys	CA044699 NM_021055.3:c.3063C>A CA394285620 NM_021055.3:c.3063C>G