Allele Registry

Canonical Allele Identifier: PA2828090646

Gene: TSC2 HGNC NCBI

ClinVar Allele:

400763

ClinVar RCV:

RCV000474153

ClinVar Variation:

406128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Asn331Asp	CA16614698 NM_001363528.2:c.991A>G