Allele Registry

Canonical Allele Identifier: PA2829981513

Gene: TSC2 HGNC NCBI

ClinVar Allele:

426155

ClinVar RCV:

RCV000497607

RCV001022632

RCV001078813

ClinVar Variation:

432500

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser1464Phe	CA394302786 NM_021055.3:c.4391C>T