Allele Registry

Canonical Allele Identifier: PA916023337

Gene: TSC2 HGNC NCBI

ClinVar Allele:

400763

ClinVar RCV:

RCV000474153

ClinVar Variation:

406128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Asn342Asp	CA16614698 NM_001318832.2:c.1024A>G