Allele Registry

Canonical Allele Identifier: PA2828093876

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000473934

RCV002323695

ClinVar Variation:

406097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Ser1268Asn	CA16615016 NM_001363528.2:c.3803G>A