Allele Registry

Canonical Allele Identifier: PA2827000841

Gene: TSC2 HGNC NCBI

ClinVar Allele:

400763

ClinVar RCV:

RCV000474153

ClinVar Variation:

406128

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Asn294Asp	CA16614698 NM_001318827.2:c.880A>G